Literature DB >> 27859606

Familial progressive hyperpigmentation and hypopigmentation without KITLG mutation.

L Zeng1,2, X D Zheng1,2, L H Liu3, L Y Fu1,2, X B Zuo1,2, G Chen1,2, P G Wang1,2, S Yang1,2, X J Zhang1,2.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2016        PMID： 27859606     DOI： 10.1111/ced.12923

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN： 0307-6938            Impact factor:   3.470


× No keyword cloud information.
  1 in total

1.  Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation.

Authors:  Jianbo Wang; Weisheng Li; Naihui Zhou; Jingliu Liu; Shoumin Zhang; Xueli Li; Zhenlu Li; Ziliang Yang; Miao Sun; Min Li
Journal:  BMC Med Genomics       Date:  2021-01-06       Impact factor: 3.063
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.