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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...
Tallennettuna:
| Julkaisussa: | Mol Med Rep |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
D.A. Spandidos
2015
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| Aiheet: | |
| Linkit: | 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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