Literature DB >> 29956681

Novel mutations in SASH1 associated with dyschromatosis universalis hereditaria.

Wei-Long Zhong1, Hui-Jun Wang2, Zhi-Miao Lin1, Yong Yang3.   

Abstract

Entities:  

Year:  2019        PMID： 29956681     DOI： 10.4103/ijdvl.IJDVL_360_17

Source DB:  PubMed          Journal:  Indian J Dermatol Venereol Leprol        ISSN： 0378-6323            Impact factor:   2.545


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  3 in total

1.  Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria.

Authors:  Jia-Wei Liu; Xiaerbati Habulieti; Rong-Rong Wang; Dong-Lai Ma; Xue Zhang
Journal:  J Clin Lab Anal       Date:  2021-05-24       Impact factor: 2.352

2.  Mutated SASH1 promotes Mitf expression in a heterozygous mutated SASH1 knock‑in mouse model.

Authors:  Zexi Xu; Yadong Li; Dahong Wang; Daoqiu Wu; Jinyun Wang; Lian Chen; Yinqian Deng; Jing Zhang; Zhixiong Wu; Xin Wan; Qianfan Liu; Hai Huang; Pingsheng Hu; Jiawei Zeng; Ding'an Zhou
Journal:  Int J Mol Med       Date:  2020-06-19       Impact factor: 4.101

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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