Literature DB >> 21571208

Dowling-Degos disease presenting as hypopigmented macules.

Tiffany L Pickup, Diya F Mutasim.   

Abstract

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Year:  2011        PMID： 21571208     DOI： 10.1016/j.jaad.2009.11.015

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN： 0190-9622            Impact factor:   11.527


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  3 in total

1.  Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos disease.

Authors:  Ming Li; Ruhong Cheng; Jianying Liang; Heng Yan; Hui Zhang; Lijia Yang; Chengrang Li; Qingqing Jiao; Zhiyong Lu; Jianhui He; Jin Ji; Zhu Shen; Chunqi Li; Fei Hao; Hong Yu; Zhirong Yao
Journal:  Am J Hum Genet       Date:  2013-05-16       Impact factor: 11.025

2.  The First Report of KRT5 Mutation Underlying Acantholytic Dowling-Degos Disease with Mottled Hypopigmentation in an Indian Family.

Authors:  Shyam Verma; Sandra M Pasternack; Arno Rütten; Thomas Ruzicka; Regina C Betz; Sandra Hanneken
Journal:  Indian J Dermatol       Date:  2014-09       Impact factor: 1.494

Review 3.  Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review).

Authors:  Jia Zhang; Ming Li; Zhirong Yao
Journal:  Mol Med Rep       Date:  2016-09-22       Impact factor: 2.952
  3 in total

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