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Male breast cancer in Cowden syndrome patients with germline PTEN mutations

Cowden syndrome (CS) (OMIM 158350) is a multiple hamartoma syndrome associated with germline mutations in the PTEN tumour suppressor gene. While CS is characterised most commonly by non-cancerous lesions (mucocutaneous trichilemmomas, acral and palmoplantar keratoses, and papillomatous papules), it...

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Autori principali: Fackenthal, J., Marsh, D., Richardson, A., Cummings, S., Eng, C., Robinson, B., Olopade, O.
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Group 2001
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734834/
https://ncbi.nlm.nih.gov/pubmed/11238682
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.38.3.159
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