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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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| Publicado no: | Mol Med Rep |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4464092/ https://ncbi.nlm.nih.gov/pubmed/25872913 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2015.3605 |
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