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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Bibliografiske detaljer
Main Authors: Angela Mauro (Author), Ebun Omoyinmi (Author), Neil James Sebire (Author), Angela Barnicoat (Author), Paul Brogan (Author)
Format: Bog
Udgivet: Hindawi Limited, 2017-01-01T00:00:00Z.
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