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Germline Epigenetic Regulation of KILLIN in Cowden and Cowden-Like Syndromes
CONTEXT: Germline loss-of-function PTEN mutations cause 80% of Cowden syndrome (CS), an autosomal dominant disorder characterized by high risks of breast, thyroid, and other cancers. A large heterogenous group of CS-like (CSL) individuals, who have various combinations of CS features but who do not...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3655326/ https://ncbi.nlm.nih.gov/pubmed/21177507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jama.2010.1877 |
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