SSCP DETECTION OF A NONSENSE MUTATION IN EXON-5 OF THE AMELOGENIN GENE (AMGX) CAUSING X-LINKED AMELOGENESIS IMPERFECTS (AIH1)

被引：63

作者：

LENCH, NJ

BROOK, AH

WINTER, GB

机构：

[1] UCL EASTMAN DENT HOSP, DEPT CHILDRENS DENT, LONDON WC1X 8LD, ENGLAND

[2] LONDON HOSP, COLL MED, SCH MED, DEPT CHILD DENT HLTH, LONDON E1 2AD, ENGLAND

来源：

HUMAN MOLECULAR GENETICS | 1994年 / 3卷 / 05期

关键词：

D O I：

10.1093/hmg/3.5.827

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：

引用

页码：827 / 828

页数：2

共 9 条

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[6] A HUMAN X-Y HOMOLOGOUS REGION ENCODES AMELOGENIN [J].

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