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

Internet

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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