AN 8-BP DELETION IN EXON-51 OF THE COL4A5 GENE OF AN ALPORT SYNDROME PATIENT

被引：10

作者：

BOYE, E ^{[1
]}

FLINTER, FA ^{[1
]}

BOBROW, M ^{[1
]}

HARRIS, A ^{[1
]}

机构：

[1] JOHN RADCLIFFE HOSP,INST MOLEC MED,DEPT PAEDIAT,OXFORD OX3 9DU,ENGLAND

来源：

HUMAN MOLECULAR GENETICS | 1993年 / 2卷 / 05期

基金：

英国医学研究理事会;

关键词：

D O I：

10.1093/hmg/2.5.595

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

页码：595 / 596

页数：2

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