Darier disease: first molecular study of a Portuguese family

BACKGROUND: Darier disease (DD) is a rare autosomal dominant condition characterized by skin lesions. Additionally, a wide range of neuropsychiatric symptoms is frequently reported in DD patients. This genodermatosis relies on mutations in the ATPase sarcoplasmic/endoplasmic reticulum Ca(2+) transpo...

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Detalles Bibliográficos
Autores principales: Almeida, Andreia, Lobo, Maria de Lurdes, Moura, Cecília, Rivera, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819764/
https://www.ncbi.nlm.nih.gov/pubmed/31687605
http://dx.doi.org/10.1016/j.heliyon.2019.e02520

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819764/
https://www.ncbi.nlm.nih.gov/pubmed/31687605
http://dx.doi.org/10.1016/j.heliyon.2019.e02520

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