Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis

被引：92

作者：

Perrault, I

Rozet, JM

Ghazi, I

Leowski, C

Bonnemaison, M

Gerber, S

Ducroq, D

Cabot, A

Souied, E

Dufier, JL

Munnich, A

Kaplan, J ^{[1
]}

机构：

[1] Hop Necker Enfants Malad, Dept Genet, INSERM, U393,Unite Rech Handicaps Genet Enfant, F-75015 Paris, France

[2] Hop Necker Enfants Malad, Serv Ophtalmol, Paris, France

[3] Inst Natl Jeunes Aveugles, Paris, France

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 64卷 / 04期

关键词：

D O I：

10.1086/302335

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1225 / 1228

页数：4

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