标题
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp
作者
关键词
-
出版物
CLINICAL AND EXPERIMENTAL DERMATOLOGY
Volume 36, Issue 2, Pages 188-194
出版商
Wiley
发表日期
2010-11-10
DOI
10.1111/j.1365-2230.2010.03944.x
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mutations in Lipase H Gene Underlie Autosomal Recessive Hypotrichosis in Five Pakistani Families
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- Homozygous Mutations in the 5′ Region of the JUP Gene Result in Cutaneous Disease but Normal Heart Development in Children
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- Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation
- (2008) Lynn Petukhova et al. GENOMICS
- Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)
- (2008) Zahid Azeem et al. HUMAN GENETICS
- Mutations in the Lipase H Gene Underlie Autosomal Recessive Woolly Hair/Hypotrichosis
- (2008) Yutaka Shimomura et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
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