Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes:: a large European study

被引:26
作者
Amaral, MD
Pacheco, P
Beck, S
Farinha, CM
Penque, D
Nogueira, P
Barreto, C
Lopes, B
Casals, T
Dapena, J
Gartner, S
Vásquez, C
Pérez-Frías, J
Olveira, C
Cabanas, R
Estivill, X
Tzetis, M
Kanavakis, E
Doudounakis, S
Dörk, T
Tümmler, B
Girodon-Boulandet, E
Cazeneuve, C
Goossens, M
Blayau, M
Verlingue, C
Vieira, I
Féréc, C
Claustres, M
des Georges, M
Clavel, C
Birembaut, P
Hubert, D
Bienvenu, T
Adoun, M
Chomel, JC
De Boeck, K
Cuppens, H
Lavinha, J
机构
[1] Inst Nacl Saude Dr Ricardo Jorge, Ctr Human Genet, P-1649016 Lisbon, Portugal
[2] Univ Lisbon, Fac Ciencias, Dept Quim & Bioquim, P-1699 Lisbon, Portugal
[3] Inst Nacl Saude Dr Ricardo Jorge, Observ Nacl Saude, P-1649016 Lisbon, Portugal
[4] Hosp Santa Maria, Serv Pediat, Unidade Fibrose Quist, Lisbon, Portugal
[5] Hosp D Estefania, Lisbon, Portugal
[6] Hosp Duran I Reynals, IRO, Dept Mol Genet, Barcelona, Spain
[7] Hosp Univ Virgen Roccio, Cyst Fibrosis Unit, Seville, Spain
[8] Hosp Univ Materno Infantil Vall Hebron, Cyst Fibrosis Unit, Barcelona, Spain
[9] Hosp Infantil Cruces, Cyst Fibrosis Unit, Pais Vasco, Spain
[10] Hosp Carlos Haya, Cyst Fibrosis Unit, Malaga, Spain
[11] Hosp Xeral Vigo, Paediat Serv, Galicia, Spain
[12] St Sophia Childrens Hosp, Dept Paediat 1, Athens, Greece
[13] St Sophia Childrens Hosp, Choremio Res Lab, Mol Med Unit, Athens, Greece
[14] Hannover Med Sch, Klin Forsch Grp, Hannover, Germany
[15] Hop Henri Mondor, Serv Biochim & genet, F-94010 Creteil, France
[16] CHRU Rennes Pontchaillou, Serv Genet Mol & Hormonol, Rennes, France
[17] CHU Brest, Lab Genet Mol & Histocompatibil, F-29285 Brest, France
[18] Inst Biol, Lab Genet Mol & Chromosom, Montpellier, France
[19] CHU Reims, Lab Pol Bouin, Reims, France
[20] CHU Reims, Hop Maison Blanche, INSERM, Unite U514, Reims, France
[21] Grp Hosp Cochin, Lab Biochim & Biol Mol, Paris, France
[22] Grp Hosp Cochin, Serv Pneumol, Paris, France
[23] CHU Poitiers, Lab Genet Cellulaire & Mol, Poitiers, France
[24] UZ Gasthuisberg, Dept Paediat, Louvain, Belgium
[25] Katholieke Univ Leuven, Ctr Human Genet, B-3001 Louvain, Belgium
关键词
D O I
10.1136/jmg.38.11.777
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:777 / 782
页数:6
相关论文
共 39 条
[11]   Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes - The polymorphic (TG)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation [J].
Cuppens, H ;
Lin, W ;
Jaspers, M ;
Costes, B ;
Teng, H ;
Vankeerberghen, A ;
Jorissen, M ;
Droogmans, G ;
Reynaert, I ;
Goossens, M ;
Nilius, B ;
Cassiman, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) :487-496
[12]   CFTR HAPLOTYPE BACKGROUNDS ON NORMAL AND MUTANT CFTR GENES [J].
CUPPENS, H ;
TENG, H ;
RAEYMAEKERS, P ;
DEBOECK, C ;
CASSIMAN, JJ .
HUMAN MOLECULAR GENETICS, 1994, 3 (04) :607-614
[13]   INTRAGENIC AND EXTRAGENIC MARKER HAPLOTYPES OF CFTR MUTATIONS IN CYSTIC-FIBROSIS FAMILIES [J].
DORK, T ;
NEUMANN, T ;
WULBRAND, U ;
WULF, B ;
KALIN, N ;
MAASS, G ;
KRAWCZAK, M ;
GUILLERMIT, H ;
FEREC, C ;
HORN, G ;
KLINGER, K ;
KEREM, BS ;
ZIELENSKI, J ;
TSUI, LC ;
TUMMLER, B .
HUMAN GENETICS, 1992, 88 (04) :417-425
[14]   FLUORESCENCE-BASED OLIGONUCLEOTIDE LIGATION ASSAY FOR ANALYSIS OF CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE-MUTATIONS [J].
EGGERDING, FA ;
IOVANNISCI, DM ;
BRINSON, E ;
GROSSMAN, P ;
WINNDEEN, ES .
HUMAN MUTATION, 1995, 5 (02) :153-165
[15]   MOLECULAR CHARACTERIZATION OF CYSTIC-FIBROSIS - 16 NOVEL MUTATIONS IDENTIFIED BY ANALYSIS OF THE WHOLE CYSTIC-FIBROSIS CONDUCTANCE TRANSMEMBRANE REGULATOR (CFTR) CODING REGIONS AND SPLICE SITE JUNCTIONS [J].
FANEN, P ;
GHANEM, N ;
VIDAUD, M ;
BESMOND, C ;
MARTIN, J ;
COSTES, B ;
PLASSA, F ;
GOOSSENS, M .
GENOMICS, 1992, 13 (03) :770-776
[16]   beta-thalassemia mutation at -90C->T impairs the interaction of the proximal CACCC box with both erythroid and nonerythroid factors [J].
Faustino, P ;
Lavinha, J ;
Marini, MG ;
Moi, P .
BLOOD, 1996, 88 (08) :3248-3249
[17]  
FERRIE RM, 1992, AM J HUM GENET, V51, P251
[18]  
Friedman KJ, 1997, HUM MUTAT, V10, P108, DOI 10.1002/(SICI)1098-1004(1997)10:2<108::AID-HUMU3>3.0.CO
[19]  
2-G
[20]   The prevalence of nasal polyps in adults with cystic fibrosis [J].
Hadfield, PJ ;
Rowe-Jones, JM ;
Mackay, IS .
CLINICAL OTOLARYNGOLOGY, 2000, 25 (01) :19-22