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Darier Disease – A Multi-organ Condition?
Darier disease is a severe, rare autosomal dominant inherited skin condition caused by mutations in the ATP2A2 gene encoding sarcoendoplasmic reticulum Ca(2+)-ATPase isoform 2 in the endoplasmic reticulum. Since sarcoendoplasmic reticulum Ca(2+)-ATPase isoform 2 is expressed in most tissues, and int...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Society for Publication of Acta Dermato-Venereologica
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364244/ https://www.ncbi.nlm.nih.gov/pubmed/33606037 http://dx.doi.org/10.2340/00015555-3770 |