A retGC-1 mutation in autosomal dominant cone-rod dystrophy

被引：72

作者：

Perrault, I

Rozet, JM

Gerber, S

Kelsell, RE

Souied, E

Cabot, A

Hunt, DM

Munnich, A

Kaplan, J

机构：

[1] Hop Necker Enfants Malad, INSERM, U393, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France

[2] UCL, Inst Ophthalmol, Dept Mol Genet, London, England

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1998年 / 63卷 / 02期

关键词：

D O I：

10.1086/301985

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：651 / 654

页数：4

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