Literature DB >> 24008101

Mutation analysis of the MVK gene in Chinese patients with disseminated superficial actinic porokeratosis.

Jingxin Dai1, Mingfei Chen, Xi'an Fu, Yongxiang Yu, Zhongxiang Shi, Changping Yu, Guangjin Wang, Hongqing Tian, Hong Liu, Furen Zhang.   

Abstract

Entities:  

Keywords:  Disseminated superficial actinic porokeratosis (DSAP); MVK; Mutation

Mesh：

Substances：

Year:  2013        PMID： 24008101     DOI： 10.1016/j.jdermsci.2013.07.011

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN： 0923-1811            Impact factor:   4.563


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  4 in total

Review 1.  Twists and turns of the genetic story of mevalonate kinase-associated diseases: A review.

Authors:  Isabelle Touitou
Journal:  Genes Dis       Date:  2021-06-09

2.  Detection of a novel missense mutation in the mevalonate kinase gene in one Chinese family with DSAP.

Authors:  Wen-Sheng Lu; Xiao-Dong Zheng; Xiu-Hua Yao; Lan-Fang Zhang; Bai Hu; Yao-Juan Lu
Journal:  Int J Clin Exp Pathol       Date:  2014-01-15

3.  A novel MVK missense mutation in one Chinese family with disseminated superficial actinic porokeratosis.

Authors:  Wen-sheng Lu; Xiao-dong Zheng; Xiu-hua Yao; Lan-fang Zhang; Mu-Qiu Wang; Fa-Xing Jiang; Si-Ping Zhang; Bai Hu
Journal:  Mol Biol Rep       Date:  2014-07-25       Impact factor: 2.316

Review 4.  Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?

Authors:  C M Mulders-Manders; A Simon
Journal:  Semin Immunopathol       Date:  2015-05-20       Impact factor: 9.623
  4 in total

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