Molecular genetics of inherited retinal degenerations

被引：14

作者：

Lindsay, Susan ^{[1
]}

Inglehearn, Christopher F. ^{[1
]}

Curtis, Ann ^{[1
]}

Bhattacharya, Shomi ^{[1
]}

机构：

[1] Univ Newcastle Upon Tyne, Mol Genet Unit, Div Human Genet, 19 Claremont Pl, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England

来源：

CURRENT OPINION IN GENETICS & DEVELOPMENT | 1992年 / 2卷 / 03期

基金：

英国惠康基金;

关键词：

D O I：

10.1016/S0959-437X(05)80158-3

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

There has recently been substantial progress in categorizing the vast range of human retinal degeneration phenotypes. A molecular approach has assigned chromosomal locations for approximately a dozen such diseases and has identifed four of the genes involved.

引用

页码：459 / 466

页数：8

共 63 条

[1]

ALDRED MA, 1991, CYTOGENET CELL GENET, V58

[2] REFINED LOCALIZATION OF THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS [J].