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De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis

Phosphatase and tensin homolog (PTEN) is the protein encoded by the PTEN gene (10q23.3). PTEN mutations are related to a variety of rare diseases referred to collectively as PTEN hamartoma tumor syndromes (PHTS), which include Cowden Syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus Syndrome, and...

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Detalles Bibliográficos
Autores principales:	Mauro, Angela, Omoyinmi, Ebun, Sebire, Neil James, Barnicoat, Angela, Brogan, Paul
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421084/ https://www.ncbi.nlm.nih.gov/pubmed/28523199 http://dx.doi.org/10.1155/2017/9682803

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