Mutation Analysis of the PTEN/MMAC1 Gene in Japanese Patients with Cowden Disease

Cowden disease (CD), also known as multiple hamartoma syndrome, is an autosomal dominant cancer syndrome associated with high risk of breast and thyroid cancer. Recently, germline mutations in PTEN/MMAC1, which has nine exons encoding a dual specificity phosphatase with homology to tensin and auxili...

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Detalles Bibliográficos
Autores principales: Sawada, Takeshi, Hamano, Naomichi, Satoh, Hiro, Okada, Toshihide, Takeda, Yasuo, Mabuchi, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2000
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926416/
https://www.ncbi.nlm.nih.gov/pubmed/10920277
http://dx.doi.org/10.1111/j.1349-7006.2000.tb01002.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926416/
https://www.ncbi.nlm.nih.gov/pubmed/10920277
http://dx.doi.org/10.1111/j.1349-7006.2000.tb01002.x

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