Literature DB >> 17635506

Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation.

T Hamada1, S Yasumoto, T Karashima, N Ishii, H Shimada, Y Kawano, S Imayama, J A McGrath, T Hashimoto.   

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Year:  2007        PMID： 17635506     DOI： 10.1111/j.1365-2133.2007.08086.x

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


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  2 in total

1.  [Darier disease].

Authors:  A Klausegger; M Laimer; J W Bauer
Journal:  Hautarzt       Date:  2013-01       Impact factor: 0.751

2.  Sporadic form of epidermolysis bullosa simplex with mottled pigmentation.

Authors:  Flávia Regina Ferreira; Carolina Fernandes Pereira; Juliana Carvalho Moretto; Mariana Patriota Naville
Journal:  An Bras Dermatol       Date:  2020-05-14       Impact factor: 1.896
  2 in total

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