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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Enregistré dans:
Détails bibliographiques
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: Nature Publishing Group 2000
Sujets:
Regular Article
Accès en ligne: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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