Screening for germline phosphatase and tensin homolog-mutations in suspected Cowden syndrome and Cowden syndrome-like families among uterine cancer patients

Cowden syndrome (CS) is an autosomal dominant disorder characterized by multiple hamartomas in the breast, thyroid and endometrium, with a prevalence of 1 per 250,000. Females with CS have a 21–28% lifetime risk of developing uterine cancer. Germline mutations in the phosphatase and tensin homolog (...

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Detalles Bibliográficos
Autores principales: TZORTZATOS, GERASIMOS, ARAVIDIS, CHRISTOS, LINDBLOM, ANNIKA, MINTS, MIRIAM, THAM, EMMA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356431/
https://www.ncbi.nlm.nih.gov/pubmed/25789042
http://dx.doi.org/10.3892/ol.2015.2890

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356431/
https://www.ncbi.nlm.nih.gov/pubmed/25789042
http://dx.doi.org/10.3892/ol.2015.2890

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