Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review

被引：2
|
作者：
Diociaiuti, A. [1 ]
Castiglia, D. [2 ]
Naim, M. [3 ]
Condorelli, A. G. [4 ]
Zambruno, G. [4 ]
El Hachem, M. [1 ]
机构：
[1] Bambino Gesu Pediat Hosp, IRCCS, Dermatol Unit, Rome, Italy
[2] IRCCS, Ist Dermopat Immacolata, Lab Mol & Cell Biol, Rome, Italy
[3] Shifa Hosp, Dermatol Sect, Gaza, Palestine
[4] Bambino Gesu Pediat Hosp, IRCCS, Genet & Rare Dis Res Area, Rome, Italy
来源：
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY | 2018年 / 32卷 / 04期
关键词：
KERATIN-14; GENE; KNOCKOUT;
D O I：
10.1111/jdv.14639
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：E149 / E151
页数：3
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