De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis
De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis
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Publisher
Cairo, Egypt: Hindawi Publishing Corporation
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Language
English
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Publisher
Cairo, Egypt: Hindawi Publishing Corporation
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Contents
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 Proteus-like syndrome. These diseases are associa...
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Full title
De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis
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TN_cdi_doaj_primary_oai_doaj_org_article_be4dd530c15f4d71ad9b449f9aa32b4d
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_be4dd530c15f4d71ad9b449f9aa32b4d
Other Identifiers
ISSN
2090-6803
E-ISSN
2090-6811
DOI
10.1155/2017/9682803
