A novel 3017-bp deletion mutation in the FERMT1 (KIND1) gene in a Chinese family with Kindler syndrome

被引：18
|
作者：
Zhou, C. [1 ]
Song, S. [2 ]
Zhang, J. [1 ]
机构：
[1] Peking Univ, Dept Dermatol, Peoples Hosp, Beijing 100871, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, Dept Med Genet, Beijing 100083, Peoples R China
来源：
BRITISH JOURNAL OF DERMATOLOGY | 2009年 / 160卷 / 05期
关键词：
deletion mutation; FERMT1; KIND1; Kindler syndrome; PROTEIN; KINDLIN-1; HOMOLOGY;
D O I：
10.1111/j.1365-2133.2009.09052.x
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
引用
收藏
页码：1119 / 1122
页数：4
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