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
Autores principales: 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: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363369/
https://www.ncbi.nlm.nih.gov/pubmed/10780518
http://dx.doi.org/10.1054/bjoc.1999.1125

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