A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations-Reference-Cited by-同舟云学术

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A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations

Published:2016-02-26 Issue:01 Volume:06 Page:e108-e111
ISSN:2157-6998
Container-title:American Journal of Perinatology Reports
language:en
Short-container-title:AJP Rep

Author:

Wakiguchi Hiroyuki¹,Maeba Shinji¹,Kimura Sasagu¹,Ito Satoko²,Tateishi Hiroshi²,Ueda Kazuhiro³,Ohga Shouichi¹,Hasegawa Shunji¹

Affiliation:

1. Department of Pediatrics, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan

2. Division of Pediatrics, JCHO Tokuyama Central Hospital, Shunan, Yamaguchi, Japan

3. Division of Pediatrics, Michigami Hospital, Hikari, Yamaguchi, Japan

Publisher

Georg Thieme Verlag KG

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1570386.pdf

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Digenic inheritance of KRT5 and KRT14 mutations in a family with epidermolysis bullosa simplex;Australasian Journal of Dermatology;2020-01-10

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