Literature DB >> 20180888

A missense mutation in KRT14 causing a dermatopathia pigmentosa reticularis/Naegeli-Franceschetti-Jadassohn phenotype.

M A M van Steensel, H H Lemmink.   

Abstract

Entities:  

Mesh：

Year:  2010        PMID： 20180888     DOI： 10.1111/j.1468-3083.2010.03598.x

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN： 0926-9959            Impact factor:   6.166


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  4 in total

1.  Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.

Authors:  Ming Li; Jianbo Wang; Zhenlu Li; Jia Zhang; Cheng Ni; Ruhong Cheng; Zhirong Yao
Journal:  Eur J Hum Genet       Date:  2016-03-02       Impact factor: 4.246

Review 2.  [Palmoplantar dermatoses: when should genes be considered?].

Authors:  C Seebode; S Schiller; S Emmert; K Giehl
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

Review 3.  Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders.

Authors:  H Alshaikh; F Alsaif; S Aldukhi
Journal:  Dermatol Res Pract       Date:  2017-10-23

4.  Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review.

Authors:  Fahad Al Saif
Journal:  Indian J Dermatol       Date:  2016 Jul-Aug       Impact factor: 1.494
  4 in total

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