OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract -: art. no. e110

被引：122

作者：

Reynier, P

Amati-Bonneau, P

Verny, C

Olichon, A

Simard, G

Guichet, A

Bonnemains, C

Malecaze, F

Malinge, MC

Pelletier, JB

Calvas, P

Dollfus, H

Belenguer, P

Malthièry, Y

Lenaers, G

Bonneau, D

机构：

[1] CHU Angers, Serv Genet Med, F-49033 Angers 01, France

[2] CHU Angers, INSERM, E0018, F-49033 Angers 01, France

[3] CHU Angers, Lab Biochim & Biol Mol, F-49033 Angers 01, France

[4] CHU Angers, Dept Neurol, F-49033 Angers 01, France

[5] Univ Toulouse 3, CNRS, UMR 5088, Lab Biol Cellulaire & Mol Controle Proliferat, F-31062 Toulouse, France

[6] CHU, INSERM, U563, Toulouse, France

[7] CHU, Serv Ophthalmol, Toulouse, France

[8] CHU, Serv Genet Med, Toulouse, France

[9] CHU Strasbourg, Serv Genet Med, F-67000 Strasbourg, France

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 09期

关键词：

D O I：

10.1136/jmg.2003.016576

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页数：6

共 27 条

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