Hereditary gynecological tumors associated with Peutz-Jeghers syndrome (Review)

Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease that is characterized by gastrointestinal hamartomatous polyposis and mucocutaneous melanin spots. The tumor suppressor gene, STK11/LKB1, which is located on chromosome 19p13.3, has been reported to be responsible for this condition. PJS...

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Detalhes bibliográficos
Main Authors: BANNO, KOUJI, KISU, IORI, YANOKURA, MEGUMI, MASUDA, KENTA, UEKI, ARISA, KOBAYASHI, YUSUKE, HIRASAWA, AKIRA, AOKI, DAISUKE
Formato: Artigo
Idioma:Inglês
Publicado em: D.A. Spandidos 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3813608/
https://ncbi.nlm.nih.gov/pubmed/24179492
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2013.1527
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