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

被引：542

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：

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

共 15 条

[1] ROLE OF PIGMENT EPITHELIUM IN ETIOLOGY OF INHERITED RETINAL DYSTROPHY IN RAT
BOK, D
HALL, MO
[J]. JOURNAL OF CELL BIOLOGY, 1971, 49 (03) : 664 - +
[2] Bourne M C, 1938, Br J Ophthalmol, V22, P613, DOI 10.1136/bjo.22.10.613
[3] BOURNE MC, 1939, J HERED, V30, P130
[4] BUNGE S, 1996, METH MOL G, V8, P26
[5] Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat
D'Cruz, PM
Yasumura, D
Weir, J
Matthes, MT
Abderrahim, H
LaVail, MM
Vollrath, D
[J]. HUMAN MOLECULAR GENETICS, 2000, 9 (04) : 645 - 651
[6] INHERITED RETINAL DYSTROPHY IN RAT
DOWLING, JE
SIDMAN, RL
[J]. JOURNAL OF CELL BIOLOGY, 1962, 14 (01) : 73 - +
[7] DEFECTIVE PHAGOCYTOSIS OF ISOLATED ROD OUTER SEGMENTS BY RCS RAT RETINAL-PIGMENT EPITHELIUM IN CULTURE
EDWARDS, RB
SZAMIER, RB
[J]. SCIENCE, 1977, 197 (4307) : 1001 - 1003
[8] PHOTORECEPTOR DEGENERATION IN INHERITED RETINAL DYSTROPHY DELAYED BY BASIC FIBROBLAST GROWTH-FACTOR
FAKTOROVICH, EG
STEINBERG, RH
YASUMURA, D
MATTHES, MT
LAVAIL, MM
[J]. NATURE, 1990, 347 (6288) : 83 - 86
[9] GRAHAM DK, 1994, CELL GROWTH DIFFER, V5, P647
[10] HERRON WL, 1969, INVEST OPHTH VISUAL, V8, P595