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KLLN epigenotype–phenotype associations in Cowden syndrome
Germline KLLN promoter hypermethylation was recently identified as a potential genetic etiology of the cancer predisposition syndrome, Cowden syndrome (CS), when no causal PTEN gene mutation was found. We screened for KLLN promoter methylation in a large prospective series of CS patients and determi...
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| Publicado en: | Eur J Hum Genet |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Nature Publishing Group
2015
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4613489/ https://ncbi.nlm.nih.gov/pubmed/25669429 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.8 |
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