MISSENSE RHODOPSIN MUTATION IN A FAMILY WITH RECESSIVE RP

被引：77

作者：

KUMARAMANICKAVEL, G

MAW, M

DENTON, MJ

JOHN, S

SRIKUMARI, CRS

ORTH, U

OEHLMANN, R

GAL, A

机构：

[1] MED RES FDN,MADRAS 600006,TAMIL NADU,INDIA

[2] INST BASIC MED SCI,DEPT GENET,MADRAS 600113,TAMIL NADU,INDIA

[3] UNIV LUBECK,INST HUMANGENET,D-23538 LUBECK,GERMANY

来源：

NATURE GENETICS | 1994年 / 8卷 / 01期

关键词：

D O I：

10.1038/ng0994-10

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：10 / 11

页数：2

共 8 条

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[7] RHODOPSIN MUTATION G90D AND A MOLECULAR MECHANISM FOR CONGENITAL NIGHT BLINDNESS [J].

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[8] A NULL MUTATION IN THE RHODOPSIN GENE CAUSES ROD PHOTORECEPTOR DYSFUNCTION AND AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA [J].

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