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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Bibliographic Details
Published in:Oncoscience
Main Authors: Yakubov, Eduard, Ghoochani, Ali, Buslei, Rolf, Buchfelder, Michael, Eyüpoglu, Ilker Y., Savaskan, Nicolai
Format: Artigo
Language:Inglês
Published: Impact Journals LLC 2016
Subjects:
Review
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4965257/
https://ncbi.nlm.nih.gov/pubmed/27489861
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncoscience.305
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