Identification of two novel Darier disease-associated mutations in the ATP2A2 gene

Darier disease (DD) is an autosomal dominant inherited skin disorder, characterized by abnormal keratinization, loss of adhesion between epidermal cells, termed acantholysis, and the development of warty papules and plaques on the central trunk, forehead, scalp and flexures. These symptoms are often...

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Detalles Bibliográficos
Autores principales: ZHENG, LIBAO, JIANG, HUILI, MEI, QIN, CHEN, BIN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464092/
https://www.ncbi.nlm.nih.gov/pubmed/25872913
http://dx.doi.org/10.3892/mmr.2015.3605

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464092/
https://www.ncbi.nlm.nih.gov/pubmed/25872913
http://dx.doi.org/10.3892/mmr.2015.3605

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