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PTEN Mutation Identified in Patient Diagnosed with Simultaneous Multiple Cancers
PTEN hamartoma tumor syndrome is a spectrum of disorders characterized by unique phenotypic features including multiple hamartomas caused by mutations of the tumor suppressor gene PTEN. Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome are representative diseases, and both have several common cl...
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| Publicado no: | Cancer Res Treat |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Cancer Association
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6333971/ https://ncbi.nlm.nih.gov/pubmed/29510612 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4143/crt.2017.579 |
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