A NOVEL CYS-214-SER MUTATION IN THE PERIPHERIN RDS GENE IN A JAPANESE FAMILY WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA

被引：52

作者：

SAGA, M ^{[1
]}

MASHIMA, Y ^{[1
]}

AKEO, K ^{[1
]}

OGUCHI, Y ^{[1
]}

KUDOH, J ^{[1
]}

SHIMIZU, N ^{[1
]}

机构：

[1] KEIO UNIV,SCH MED,DEPT MOLEC BIOL,SHINJUKU KU,TOKYO 160,JAPAN

来源：

HUMAN GENETICS | 1993年 / 92卷 / 05期

关键词：

D O I：

10.1007/BF00216463

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

We have screened for possible disease-causing mutations in the peripherin/retinal degeneration slow (RDS) gene in 13 Japanese families with autosomal dominant retinitis pigmentosa (ADRP). Using polymerase chain reaction-single strand conformation polymorphism analysis, a novel mutation at codon 214 was found in which the highly conserved cysteine was replaced with a serine in one family. The mutation at codon 214 was found in all three affected siblings of this family, but none of the 40 normal control individuals had this mutation. These results strongly suggest that the mutation is pathogenic for RP in this family. The clinical phenotype for this family is a late-onset form of ADRP.

引用

页码：519 / 521

页数：3

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