Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study

被引：93

作者：

Hardcastle, AJ

Thiselton, DL

Van Maldergem, L

Saha, BK

Jay, M

Plant, C

Taylor, R

Bird, AC

Bhattacharya, S

机构：

[1] UCL, Inst Ophthalmol, Dept Mol Genet, London EC1V 9EL, England

[2] UCL, Inst Ophthalmol, Dept Clin Ophthalmol, London, England

[3] Inst Pathol & Genet ASBL, Gerpinnes, Belgium

[4] Emory Univ, Sch Med, Winship Canc Ctr, Atlanta, GA 30322 USA

来源：

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

关键词：

D O I：

10.1086/302325

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1210 / 1215

页数：6

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