Literature DB >> 30430618

Atypical presentation of dyschromatosis universalis hereditaria with a novel ABCB6 mutation.

W Zhong1,2, Y Pan1,2, Y Shao3, Y Yang1,2,4, B Yu3, Z Lin1,2.   

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Year:  2018        PMID： 30430618     DOI： 10.1111/ced.13833

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


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  3 in total

1.  Identification of two novel mutations in the PLCD1 gene in Chinese patients with hereditary leukonychia.

Authors:  Shuzhan Shen; Minhua Shao; Uma Keyal; Xiuli Wang; Ming Li; Guolong Zhang
Journal:  Mol Med Rep       Date:  2021-03-31       Impact factor: 2.952

2.  Inhibition of Fam114A1 protects melanocytes from apoptosis through higher RACK1 expression.

Authors:  Miaoni Zhou; Fuquan Lin; Xingang Wu; Zhuyi Ping; Wen Xu; Rong Jin; Aie Xu
Journal:  Aging (Albany NY)       Date:  2021-11-27       Impact factor: 5.682

3.  Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria.

Authors:  Lu Cao; Ruixue Zhang; Liang Yong; Shirui Chen; Hui Zhang; Weiwei Chen; Qiongqiong Xu; Huiyao Ge; Yiwen Mao; Qi Zhen; Yafen Yu; Xia Hu; Liangdan Sun
Journal:  BMC Med Genomics       Date:  2021-06-26       Impact factor: 3.063
  3 in total

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