Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

被引：548

作者：

Gal, A

Li, Y

Thompson, DA

Weir, J

Orth, U

Jacobson, SG

Apfelstedt-Sylla, E

Vollrath, D ^{[1
]}

机构：

[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA

[2] Univ Michigan, Sch Med, Dept Ophthalmol & Visual Sci, Ann Arbor, MI USA

[3] Univ Michigan, Sch Med, Dept Biol Chem, Ann Arbor, MI 48109 USA

[4] Univ Krankenhaus Eppendorf, Inst Human Genet, Hamburg, Germany

[5] Univ Penn, Scheie Eye Inst, Dept Ophthalmol, Philadelphia, PA 19104 USA

[6] Univ Eye Clin, Dept Pathophysiol Vis & Neuroophthalmol, Tubingen, Germany

来源：

NATURE GENETICS | 2000年 / 26卷 / 03期

关键词：

D O I：

10.1038/81555

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：270 / 271

页数：2

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[8] PHOTORECEPTOR DEGENERATION IN INHERITED RETINAL DYSTROPHY DELAYED BY BASIC FIBROBLAST GROWTH-FACTOR [J].

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