Case report of two siblings with a novel homozygous mutation in COL7A1 leads to recessive dystrophic epidermolysis bullosa: which type?

被引：1
|
作者：
Gumus, Evren [1 ]
机构：
[1] Univ Harran, Fac Med, Dept Med Genet, TR-63000 Sanliurfa, Turkey
来源：
CLINICAL DYSMORPHOLOGY | 2018年 / 27卷 / 04期
关键词：
CLASSIFICATION;
D O I：
10.1097/MCD.0000000000000229
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页码：138 / 141
页数：4
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