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Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome

Peutz-Jeghers syndrome (PJS), a rare autosomal dominant inherited disorder, is characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation. Patients with this syndrome have a predisposition to a variety of cancers in multiple organs. Mutations in the serine/threonine kinase...

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Autores principales: Ausavarat, Surasawadee, Leoyklang, Petcharat, Vejchapipat, Paisarn, Chongsrisawat, Voranush, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk
Formato: Artigo
Lenguaje:Inglês
Publicado: The WJG Press and Baishideng 2009
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2776867/
https://ncbi.nlm.nih.gov/pubmed/19908348
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.15.5364
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