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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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| Publicado no: | Jpn J Cancer Res |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Ltd
2000
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5926416/ https://ncbi.nlm.nih.gov/pubmed/10920277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1349-7006.2000.tb01002.x |
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