Literature DB >> 31912549

Erythrokeratodermia variabilis et progressiva with a rare GJB3 mutation.

Kie Imura1, Shigeki Ikeya1, Tsutomu Ogata2, Yoshiki Tokura1.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2020        PMID： 31912549     DOI： 10.1111/1346-8138.15206

Source DB:  PubMed          Journal:  J Dermatol        ISSN： 0385-2407            Impact factor:   4.005


× No keyword cloud information.
  1 in total

1.  A Connexin Gene (GJB3) Mutation in a Chinese Family With Erythrokeratodermia Variabilis, Ichthyosis and Nonsyndromic Hearing Loss: Case Report and Mutations Update.

Authors:  Yajuan Gao; Qianli Zhang; Shiyu Zhang; Lu Yang; Yaping Liu; Yuehua Liu; Tao Wang
Journal:  Front Genet       Date:  2022-05-23       Impact factor: 4.772
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.