A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

被引：172
|
作者：
Bessant, DAR
Payne, AM
Mitton, KP
Wang, QL
Swain, PK
Plant, C
Bird, AC
Zack, DJ
Swaroop, A
Bhattacharya, SS [1 ]
机构：
[1] UCL, Inst Ophthalmol, Dept Mol Genet, London, England
[2] Moorfields Eye Hosp, London, England
[3] Univ Michigan, WK Kellogg Eye Ctr, Dept Ophthalmol, Ann Arbor, MI 48105 USA
[4] Univ Michigan, WK Kellogg Eye Ctr, Dept Human Genet, Ann Arbor, MI 48105 USA
[5] Johns Hopkins Univ, Sch Med, Dept Ophthalmol, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
来源：
NATURE GENETICS | 1999年 / 21卷 / 04期
关键词：
D O I：
10.1038/7678
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：355 / 356
页数：2
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