Hidden association of Cowden syndrome, PTEN mutation and meningioma frequency

Cowden syndrome (CS) is clinically presented by multiple hamartomas, often with mucocutaneous lesions, goiter, breast cancer and gastrointestinal polyps. CS is a genetic disorder of autosomal dominant inheritance and is one distinct syndrome of the phosphatase and tensin homolog on chromosome 10 (PT...

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Detalles Bibliográficos
Autores principales: Yakubov, Eduard, Ghoochani, Ali, Buslei, Rolf, Buchfelder, Michael, Eyüpoglu, Ilker Y., Savaskan, Nicolai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965257/
https://www.ncbi.nlm.nih.gov/pubmed/27489861
http://dx.doi.org/10.18632/oncoscience.305

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965257/
https://www.ncbi.nlm.nih.gov/pubmed/27489861
http://dx.doi.org/10.18632/oncoscience.305

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