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Prevalence of Mitochondrial 1555A>G Mutation in Adults of European Descent
被引:88
作者
:
Vandebona, Himesha
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Vandebona, Himesha
[
1
]
Mitchell, Paul
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Ctr Vis Res, Sydney, NSW 2145, Australia
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Mitchell, Paul
[
2
]
Manwaring, Neil
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Manwaring, Neil
[
1
]
Griffiths, Kate
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Griffiths, Kate
[
1
]
Gopinath, Bamini
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Ctr Vis Res, Sydney, NSW 2145, Australia
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Gopinath, Bamini
[
2
]
Wang, Jie Jin
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Ctr Vis Res, Sydney, NSW 2145, Australia
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Wang, Jie Jin
[
2
]
Sue, Carolyn M.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
Sue, Carolyn M.
[
1
]
机构
:
[1]
Univ Sydney, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
[2]
Univ Sydney, Ctr Vis Res, Sydney, NSW 2145, Australia
来源
:
NEW ENGLAND JOURNAL OF MEDICINE
|
2009年
/ 360卷
/ 06期
关键词
:
HEARING-LOSS;
DEAFNESS;
D O I
:
10.1056/NEJMc0806397
中图分类号
:
R5 [内科学];
学科分类号
:
1002 ;
100201 ;
摘要
:
引用
收藏
页码:642 / 644
页数:3
相关论文
共 6 条
[1]
Hereditary deafness and phenotyping in humans
Bitner-Glindzicz, M
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Unit Clin & Mol Genet, London WC1N 1EH, England
Inst Child Hlth, Unit Clin & Mol Genet, London WC1N 1EH, England
Bitner-Glindzicz, M
[J].
BRITISH MEDICAL BULLETIN,
2002,
63
: 73
-
94
[2]
Prevalence of Mitochondrial 1555A>G Mutation in European Children
Bitner-Glindzicz, Maria
论文数:
0
引用数:
0
h-index:
0
机构:
UCL Inst Child Hlth, London WC1N 1EH, England
UCL Inst Child Hlth, London WC1N 1EH, England
Bitner-Glindzicz, Maria
Pembrey, Marcus
论文数:
0
引用数:
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h-index:
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UCL Inst Child Hlth, London WC1N 1EH, England
UCL Inst Child Hlth, London WC1N 1EH, England
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h-index:
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UCL Inst Child Hlth, London WC1N 1EH, England
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Ring, Susan M.
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MRC, Ctr Neuromuscular Dis, London WC1N 3BG, England
UCL Inst Child Hlth, London WC1N 1EH, England
Rahman, Shamima
[J].
NEW ENGLAND JOURNAL OF MEDICINE,
2009,
360
(06)
: 640
-
642
[3]
Mitochondrial DNA haplogroups and age-related hearing loss
Manwaring, Neil
论文数:
0
引用数:
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Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
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Rochtchina, Elena
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0
h-index:
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Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
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[J].
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133
(09)
: 929
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933
[4]
Population prevalence of the MELAS A3243G mutation
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Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
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Jones, Michael M.
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h-index:
0
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Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
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[J].
MITOCHONDRION,
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(03)
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[5]
MITOCHONDRIAL RIBOSOMAL-RNA MUTATION ASSOCIATED WITH BOTH ANTIBIOTIC-INDUCED AND NON-SYNDROMIC DEAFNESS
PREZANT, TR
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0
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CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
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ROTTER, JI
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CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
FISCHELGHODSIAN, N
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Cochlear origin of hearing loss in MELAS syndrome
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Morris, JGL
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ANNALS OF NEUROLOGY,
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←
1
→
共 6 条
[1]
Hereditary deafness and phenotyping in humans
Bitner-Glindzicz, M
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Unit Clin & Mol Genet, London WC1N 1EH, England
Inst Child Hlth, Unit Clin & Mol Genet, London WC1N 1EH, England
Bitner-Glindzicz, M
[J].
BRITISH MEDICAL BULLETIN,
2002,
63
: 73
-
94
[2]
Prevalence of Mitochondrial 1555A>G Mutation in European Children
Bitner-Glindzicz, Maria
论文数:
0
引用数:
0
h-index:
0
机构:
UCL Inst Child Hlth, London WC1N 1EH, England
UCL Inst Child Hlth, London WC1N 1EH, England
Bitner-Glindzicz, Maria
Pembrey, Marcus
论文数:
0
引用数:
0
h-index:
0
机构:
UCL Inst Child Hlth, London WC1N 1EH, England
UCL Inst Child Hlth, London WC1N 1EH, England
Pembrey, Marcus
Duncan, Andrew
论文数:
0
引用数:
0
h-index:
0
机构:
UCL Inst Child Hlth, London WC1N 1EH, England
UCL Inst Child Hlth, London WC1N 1EH, England
Duncan, Andrew
论文数:
引用数:
h-index:
机构:
Heron, Jon
Ring, Susan M.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Bristol BS8 1TH, Avon, England
UCL Inst Child Hlth, London WC1N 1EH, England
Ring, Susan M.
Hall, Amanda
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Bristol BS8 1TH, Avon, England
UCL Inst Child Hlth, London WC1N 1EH, England
Hall, Amanda
Rahman, Shamima
论文数:
0
引用数:
0
h-index:
0
机构:
MRC, Ctr Neuromuscular Dis, London WC1N 3BG, England
UCL Inst Child Hlth, London WC1N 1EH, England
Rahman, Shamima
[J].
NEW ENGLAND JOURNAL OF MEDICINE,
2009,
360
(06)
: 640
-
642
[3]
Mitochondrial DNA haplogroups and age-related hearing loss
Manwaring, Neil
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
Manwaring, Neil
Jones, Michael M.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
Jones, Michael M.
Wang, Jie Jin
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
Wang, Jie Jin
Rochtchina, Elena
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
Rochtchina, Elena
Howard, Chris
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
Howard, Chris
Newall, Phillip
论文数:
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引用数:
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h-index:
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机构:
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Mitchell, Paul
论文数:
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引用数:
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h-index:
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Mitchell, Paul
Sue, Carolyn M.
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0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst, Dept Neurogenet, Sydney, NSW 2006, Australia
Sue, Carolyn M.
[J].
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY,
2007,
133
(09)
: 929
-
933
[4]
Population prevalence of the MELAS A3243G mutation
Manwaring, Neil
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
Manwaring, Neil
Jones, Michael M.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
Jones, Michael M.
Wang, Jie Jin
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
Wang, Jie Jin
Rochtchina, Elena
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
Rochtchina, Elena
Howard, Chris
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
Howard, Chris
Mitchell, Paul
论文数:
0
引用数:
0
h-index:
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机构:
Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
Mitchell, Paul
Sue, Carolyn M.
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0
引用数:
0
h-index:
0
机构:
Univ Sydney, Kolling Inst Med Res, Dept Neurogenet, Royal N Shore Hosp, St Leonards, NSW 2065, Australia
Sue, Carolyn M.
[J].
MITOCHONDRION,
2007,
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(03)
: 230
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233
[5]
MITOCHONDRIAL RIBOSOMAL-RNA MUTATION ASSOCIATED WITH BOTH ANTIBIOTIC-INDUCED AND NON-SYNDROMIC DEAFNESS
PREZANT, TR
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0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
PREZANT, TR
AGAPIAN, JV
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
AGAPIAN, JV
BOHLMAN, MC
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
BOHLMAN, MC
BU, XD
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
BU, XD
OZTAS, S
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
OZTAS, S
QIU, WQ
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
QIU, WQ
ARNOS, KS
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
ARNOS, KS
CORTOPASSI, GA
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
CORTOPASSI, GA
JABER, L
论文数:
0
引用数:
0
h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
JABER, L
ROTTER, JI
论文数:
0
引用数:
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h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
ROTTER, JI
SHOHAT, M
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引用数:
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h-index:
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机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
SHOHAT, M
FISCHELGHODSIAN, N
论文数:
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引用数:
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h-index:
0
机构:
CEDARS SINAI MED CTR, CTR MED GENET BIRTH DEFECTS, STEVEN SPIELBERG PEDIAT RES CTR, LOS ANGELES, CA 90048 USA
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