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AAV Gene Therapy for Autosomal Dominant Optic Atrophy Caused by Mutation in the Opa1 Gene
被引:0
作者
:
Stupay, Rachel M.
论文数:
0
引用数:
0
h-index:
0
机构:
Abeona Therapeut, Product Dev, Cleveland, OH USA
Abeona Therapeut, Product Dev, Cleveland, OH USA
Stupay, Rachel M.
[
1
]
Cascone, Alyna
论文数:
0
引用数:
0
h-index:
0
机构:
Abeona Therapeut, Product Dev, Cleveland, OH USA
Abeona Therapeut, Product Dev, Cleveland, OH USA
Cascone, Alyna
[
1
]
Padegimas, Linas
论文数:
0
引用数:
0
h-index:
0
机构:
Forge Biol, Grove City, OH USA
Abeona Therapeut, Product Dev, Cleveland, OH USA
Padegimas, Linas
[
2
]
Wille, Paul T.
论文数:
0
引用数:
0
h-index:
0
机构:
Abeona Therapeut, Product Dev, Cleveland, OH USA
Abeona Therapeut, Product Dev, Cleveland, OH USA
Wille, Paul T.
[
1
]
Kevany, Brian M.
论文数:
0
引用数:
0
h-index:
0
机构:
Abeona Therapeut, Cleveland, OH USA
Abeona Therapeut, Product Dev, Cleveland, OH USA
Kevany, Brian M.
[
3
]
机构
:
[1]
Abeona Therapeut, Product Dev, Cleveland, OH USA
[2]
Forge Biol, Grove City, OH USA
[3]
Abeona Therapeut, Cleveland, OH USA
来源
:
MOLECULAR THERAPY
|
2023年
/ 31卷
/ 04期
关键词
:
D O I
:
暂无
中图分类号
:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号
:
071005 ;
0836 ;
090102 ;
100705 ;
摘要
:
1478
引用
收藏
页码:696 / 697
页数:2
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共 50 条
[31]
First report of OPA1 screening in Greek patients with autosomal dominant optic atrophy and identification of a previously undescribed OPA1 mutation
Kamakari, Smaragda
论文数:
0
引用数:
0
h-index:
0
机构:
OMMA Ophthalmol Inst Athens, Ophthalm Genet Unit, Athens, Greece
OMMA Ophthalmol Inst Athens, Ophthalm Genet Unit, Athens, Greece
Kamakari, Smaragda
Koutsodontis, George
论文数:
0
引用数:
0
h-index:
0
机构:
OMMA Ophthalmol Inst Athens, Ophthalm Genet Unit, Athens, Greece
OMMA Ophthalmol Inst Athens, Ophthalm Genet Unit, Athens, Greece
Koutsodontis, George
Tsilimbaris, Miltiadis
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Crete, Sch Med, Dept Ophthalmol, Iraklion, Greece
OMMA Ophthalmol Inst Athens, Ophthalm Genet Unit, Athens, Greece
Tsilimbaris, Miltiadis
Fitsios, Athanasios
论文数:
0
引用数:
0
h-index:
0
机构:
MITERA Childrens Hosp, Pediat Ophthalmol Dept, Athens, Greece
OMMA Ophthalmol Inst Athens, Ophthalm Genet Unit, Athens, Greece
Fitsios, Athanasios
Chrousos, Georgia
论文数:
0
引用数:
0
h-index:
0
机构:
MITERA Childrens Hosp, Pediat Ophthalmol Dept, Athens, Greece
OMMA Ophthalmol Inst Athens, Ophthalm Genet Unit, Athens, Greece
Chrousos, Georgia
MOLECULAR VISION,
2014,
20
: 691
-
703
[32]
Peripapillary capillary network in dominant optic atrophy linked to OPA1 gene
Rahhal-Ortuno, Miriam
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Rahhal-Ortuno, Miriam
Avino-Martinez, Juan Aurelio
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Avino-Martinez, Juan Aurelio
Fernandez-Santodomingo, Alex Samir
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Fernandez-Santodomingo, Alex Samir
Aguilar-Gonzalez, Marina
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Aguilar-Gonzalez, Marina
Placinta-Tat, Ioan Alexandru
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Placinta-Tat, Ioan Alexandru
Espana-Gregori, Enrique
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Hosp Univ & Politecn La Fe, Dept Ophthalmol, Avinguda Fernando Abril Martorell 106, Valencia 46026, Valencian Commu, Spain
Espana-Gregori, Enrique
EUROPEAN JOURNAL OF OPHTHALMOLOGY,
2023,
33
(01)
: NP19
-
NP22
[33]
Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene
Granse, L
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lund Hosp, Dept Ophthalmol, S-22185 Lund, Sweden
Granse, L
Bergstrand, I
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lund Hosp, Dept Ophthalmol, S-22185 Lund, Sweden
Bergstrand, I
Thiselton, D
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lund Hosp, Dept Ophthalmol, S-22185 Lund, Sweden
Thiselton, D
Ponjavic, V
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lund Hosp, Dept Ophthalmol, S-22185 Lund, Sweden
Ponjavic, V
Heijl, A
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lund Hosp, Dept Ophthalmol, S-22185 Lund, Sweden
Heijl, A
Votruba, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lund Hosp, Dept Ophthalmol, S-22185 Lund, Sweden
Votruba, M
Andréasson, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Lund Hosp, Dept Ophthalmol, S-22185 Lund, Sweden
Andréasson, S
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE,
2003,
44
: U446
-
U446
[34]
The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene
Amati-Bonneau, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Angers, Lab Biochim & Biol Mol, F-49100 Angers, France
Amati-Bonneau, P
Odent, S
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Angers, Lab Biochim & Biol Mol, F-49100 Angers, France
Odent, S
Derrien, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Angers, Lab Biochim & Biol Mol, F-49100 Angers, France
Derrien, C
Pasquier, L
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Angers, Lab Biochim & Biol Mol, F-49100 Angers, France
Pasquier, L
Malthiéry, Y
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Angers, Lab Biochim & Biol Mol, F-49100 Angers, France
Malthiéry, Y
Reynier, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Angers, Lab Biochim & Biol Mol, F-49100 Angers, France
Reynier, P
Bonneau, D
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Angers, Lab Biochim & Biol Mol, F-49100 Angers, France
Bonneau, D
AMERICAN JOURNAL OF OPHTHALMOLOGY,
2003,
136
(06)
: 1170
-
1171
[35]
Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy
Fuhrmann, N.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Fuhrmann, N.
Alavi, M. V.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Alavi, M. V.
Bitoun, P.
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Paris Nord, Genet Med Hop Jean Verdier, Bondy, France
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Bitoun, P.
Woernle, S.
论文数:
0
引用数:
0
h-index:
0
机构:
Clin Ctr Traunstein, Dept Pediat, Traunstein, Germany
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Woernle, S.
Auburger, G.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Clin Frankfurt, Dept Neurol, Sect Mol Neurogenet, Frankfurt, Germany
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Auburger, G.
Leo-Kottler, B.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Clin Tuebingen, Ctr Ophthalmol, Univ Eye Hosp, Tubingen, Germany
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Leo-Kottler, B.
Yu-Wai-Man, P.
论文数:
0
引用数:
0
h-index:
0
机构:
Newcastle Univ, Sch Med, Mitochondrial Res Grp, Newcastle Upon Tyne, Tyne & Wear, England
Royal Victoria Infirm, Dept Ophthalmol, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Yu-Wai-Man, P.
Chinnery, P.
论文数:
0
引用数:
0
h-index:
0
机构:
Newcastle Univ, Sch Med, Mitochondrial Res Grp, Newcastle Upon Tyne, Tyne & Wear, England
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Chinnery, P.
Wissinger, B.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Univ Clin Tuebingen, Mol Genet Lab, Inst Ophthalm Res, Ctr Ophthalmol, D-72076 Tubingen, Germany
Wissinger, B.
JOURNAL OF MEDICAL GENETICS,
2009,
46
(02)
: 136
-
144
[36]
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts
Zanfardino, Paola
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Zanfardino, Paola
Amati, Alessandro
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Amati, Alessandro
Doccini, Stefano
论文数:
0
引用数:
0
h-index:
0
机构:
IRCCS Stella Maris Fdn, Mol Med Neurodegenerat & Neuromuscular Dis Unit, Viale Tirreno, I-56128 Pisa, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Doccini, Stefano
Cox, Sharon N.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Study Bari Aldo Moro, Dept Biosci Biotechnol & Biopharmaceut, via Orabona 4, I-70125 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Cox, Sharon N.
Tullo, Apollonia
论文数:
0
引用数:
0
h-index:
0
机构:
CNR, Inst Biomembranes Bioenerget & Mol Biotechnol IBIO, Via G Amendola 122-O, I-70126 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Tullo, Apollonia
Longo, Giovanna
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Longo, Giovanna
D'Erchia, Annamaria
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Study Bari Aldo Moro, Dept Biosci Biotechnol & Biopharmaceut, via Orabona 4, I-70125 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
D'Erchia, Annamaria
Picardi, Ernesto
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Study Bari Aldo Moro, Dept Biosci Biotechnol & Biopharmaceut, via Orabona 4, I-70125 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Picardi, Ernesto
Nesti, Claudia
论文数:
0
引用数:
0
h-index:
0
机构:
IRCCS Stella Maris Fdn, Mol Med Neurodegenerat & Neuromuscular Dis Unit, Viale Tirreno, I-56128 Pisa, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Nesti, Claudia
Santorelli, Filippo M.
论文数:
0
引用数:
0
h-index:
0
机构:
IRCCS Stella Maris Fdn, Mol Med Neurodegenerat & Neuromuscular Dis Unit, Viale Tirreno, I-56128 Pisa, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Santorelli, Filippo M.
Petruzzella, Vittoria
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Univ Study Bari Aldo Moro, Dept Translat Biomed & Neurosci DiBraiN, Piazza G Cesare 11, I-70124 Bari, Italy
Petruzzella, Vittoria
HUMAN MOLECULAR GENETICS,
2024,
33
(09)
: 768
-
786
[37]
OPA1 mutations and mitochondrial DNA haplotypes in autosomal dominant optic atrophy
Han, J
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Han, J
Thompson-Lowrey, AJ
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Thompson-Lowrey, AJ
Reiss, A
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Reiss, A
Mayorov, V
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Mayorov, V
Jlia, H
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Jlia, H
Biousse, V
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Biousse, V
Newman, NJ
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Newman, NJ
Brown, MD
论文数:
0
引用数:
0
h-index:
0
机构:
Mercer Univ, Sch Med, Dept Basic Med Sci, Macon, GA 31207 USA
Brown, MD
GENETICS IN MEDICINE,
2006,
8
(04)
: 217
-
225
[38]
Autosomal dominant optic atrophy:: Penetrance and expressivity in patients with OPA1 mutations
Cohn, Amn C.
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Victorian Eye & Ear Hosp, Ocular Diagnost Clin, Melbourne, Vic 3002, Australia
Cohn, Amn C.
论文数:
引用数:
h-index:
机构:
Toomes, Carmel
Potter, Catherine
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Victorian Eye & Ear Hosp, Ocular Diagnost Clin, Melbourne, Vic 3002, Australia
Potter, Catherine
Towns, Katherine V.
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Victorian Eye & Ear Hosp, Ocular Diagnost Clin, Melbourne, Vic 3002, Australia
Towns, Katherine V.
Hewitt, Alex W.
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Victorian Eye & Ear Hosp, Ocular Diagnost Clin, Melbourne, Vic 3002, Australia
Hewitt, Alex W.
Inglehearn, Chris F.
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Victorian Eye & Ear Hosp, Ocular Diagnost Clin, Melbourne, Vic 3002, Australia
Inglehearn, Chris F.
Craig, Jamie E.
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Victorian Eye & Ear Hosp, Ocular Diagnost Clin, Melbourne, Vic 3002, Australia
Craig, Jamie E.
Mackey, David A.
论文数:
0
引用数:
0
h-index:
0
机构:
Royal Victorian Eye & Ear Hosp, Ocular Diagnost Clin, Melbourne, Vic 3002, Australia
Mackey, David A.
AMERICAN JOURNAL OF OPHTHALMOLOGY,
2007,
143
(04)
: 656
-
662
[39]
A novel mutation of the OPA1 gene in a Japanese family with optic atrophy type 1
Shimizu, S
论文数:
0
引用数:
0
h-index:
0
机构:
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Shimizu, S
Mori, N
论文数:
0
引用数:
0
h-index:
0
机构:
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Mori, N
Kishi, M
论文数:
0
引用数:
0
h-index:
0
机构:
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Kishi, M
Sugata, H
论文数:
0
引用数:
0
h-index:
0
机构:
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Sugata, H
Tsuda, A
论文数:
0
引用数:
0
h-index:
0
机构:
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Tsuda, A
Kubota, N
论文数:
0
引用数:
0
h-index:
0
机构:
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Teikyo Univ, Sch Med, Dept Ophthalmol, Itabashi Ku, Tokyo 1738605, Japan
Kubota, N
JAPANESE JOURNAL OF OPHTHALMOLOGY,
2002,
46
(03)
: 336
-
340
[40]
Sex-influenced autosomal dominant optic atrophy is caused by mutations of IVS9+2A>G in the OPA1 gene
Huang, TS
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
Huang, TS
Whang, JD
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
Whang, JD
Kimonis, V
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
Kimonis, V
GENETICS IN MEDICINE,
2006,
8
(01)
: 59
-
59
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