Literature DB >> 24024749

Coexistence of KRT14 and KRT5 mutations in a Polish patient with epidermolysis bullosa simplex.

K Wertheim-Tysarowska1, J Sota, A Kutkowska-Kaźmierczak, K Woźniak, J Bal, C Kowalewski.   

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Year:  2014        PMID： 24024749     DOI： 10.1111/bjd.12624

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  2 in total

1.  A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations.

Authors:  Hiroyuki Wakiguchi; Shunji Hasegawa; Shinji Maeba; Sasagu Kimura; Satoko Ito; Hiroshi Tateishi; Kazuhiro Ueda; Shouichi Ohga
Journal:  AJP Rep       Date:  2016-03

2.  Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlation.

Authors:  K Wertheim-Tysarowska; M Ołdak; A Giza; A Kutkowska-Kaźmierczak; J Sota; D Przybylska; K Woźniak; D Śniegórska; K Niepokój; A Sobczyńska-Tomaszewska; A M Rygiel; R Płoski; J Bal; C Kowalewski
Journal:  J Appl Genet       Date:  2015-10-02       Impact factor: 3.240
  2 in total

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