Germline mutations of the STK11 gene in Korean Peutz–Jeghers syndrome patients

Peutz–Jeghers syndrome (PJS) is an autosomal dominantly inherited disease characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation, with an increased risk for various neoplasms, including gastrointestinal cancer. Recently, the PJS gene encoding the serine/threonine kinas...

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Detalles Bibliográficos
Main Authors: Yoon, K-A, Ku, J-L, Choi, H S, Heo, S C, Jeong, S-Y, Park, Y J, Kim, N K, Kim, J C, Jung, P M, Park, J-G
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group 2000
Assuntos:
Regular Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2363369/
https://ncbi.nlm.nih.gov/pubmed/10780518
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1054/bjoc.1999.1125
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