Mutations in RPE65 cause Leber's congenital amaurosis

被引：470

作者：

Marlhens, F

Bareil, C

Griffoin, JM

Zrenner, E

Amalric, P

Eliaou, C

Liu, SY

Harris, E

Redmond, TM

Arnaud, B

Claustres, M

Hamel, CP

机构：

[1] HOP ST CHARLES,LAB NEUROBIOL AUDIT PLAST SYNAPT,INSERM,U254,F-34295 MONTPELLIER 5,FRANCE

[2] INST BIOL,BIOCHIM GENET LAB,MONTPELLIER,FRANCE

[3] UNIV TUBINGEN,HOSP EYE,TUBINGEN,GERMANY

[4] CABINET OPTHALMOL,ALBI,FRANCE

[5] HOP GUI DE CHAULIAC,SERV OPTALMOL,MONTPELLIER,FRANCE

[6] NEI,RETINAL CELL & MOL BIOL LAB,NIH,BETHESDA,MD 20892

来源：

NATURE GENETICS | 1997年 / 17卷 / 02期

关键词：

D O I：

10.1038/ng1097-139

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：139 / 141

页数：3

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