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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Sparad:
Bibliografiska uppgifter
I publikationen:Oncoscience
Huvudupphovsmän: Yakubov, Eduard, Ghoochani, Ali, Buslei, Rolf, Buchfelder, Michael, Eyüpoglu, Ilker Y., Savaskan, Nicolai
Materialtyp: Artigo
Språk:Inglês
Publicerad: Impact Journals LLC 2016
Ämnen:
Review
Länkar: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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