Novel serine/threonine kinase 11 gene mutations in Peutz-Jeghers syndrome patients and endoscopic management

AIM: To explore mutations in serine/threonine kinase 11 (STK11) gene in Peutz-Jeghers syndrome (PJS) with gastrointestinal (GI) hamartomatous polyps. METHODS: Six Japanese PJS patients in 3 families were enrolled in this study. Each of the cases had hamartomatous polyposis in the gastrointestinal tr...

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Detaylı Bibliyografya
Asıl Yazarlar: Yajima, Hiroyuki, Isomoto, Hajime, Nishioka, Hiroaki, Yamaguchi, Naoyuki, Ohnita, Ken, Ichikawa, Tatsuki, Takeshima, Fuminao, Shikuwa, Saburo, Ito, Masahiro, Nakao, Kazuhiko, Tsukamoto, Kazuhiro, Kohno, Shigeru
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Baishideng Publishing Group Co., Limited 2013
Konular:
Brief Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3600545/
https://ncbi.nlm.nih.gov/pubmed/23515270
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4253/wjge.v5.i3.102
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