MUTATIONS IN THE HUMAN PERIPHERIN/RDS GENE ASSOCIATED WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA

被引：31

作者：

GRUNING, G

MILLAN, JM

MEINS, M

BENEYTO, M

CABALLERO, M

APFELSTEDTSYLLA, E

BOSCH, R

ZRENNER, E

PRIETO, F

GAL, A

机构：

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

[2] UNIV VALENCIA,HOSP LA FE,UNIDAD GENET & DIAGNOST PRENATAL,E-46009 VALENCIA,SPAIN

[3] UNIV TUBINGEN,AUGENKLIN,D-72076 TUBINGEN,GERMANY

来源：

HUMAN MUTATION | 1994年 / 3卷 / 03期

关键词：

D O I：

10.1002/humu.1380030326

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：321 / 323

页数：3

共 8 条

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[5] A 2 BASE-PAIR DELETION IN THE RDS GENE ASSOCIATED WITH BUTTERFLY-SHAPED PIGMENT DYSTROPHY OF THE FOVEA [J].

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[6] THE HUMAN RETINAL DEGENERATION SLOW (RDS) GENE - CHROMOSOME ASSIGNMENT AND STRUCTURE OF THE MESSENGER-RNA [J].

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[7] A MEDLEY OF RETINAL DYSTROPHIES [J].

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[8] MUTATIONS IN THE HUMAN RETINAL DEGENERATION SLOW (RDS) GENE CAN CAUSE EITHER RETINITIS-PIGMENTOSA OR MACULAR DYSTROPHY [J].

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