Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.

Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigmentation and hamartomatous polyps. There is an increased risk of benign and malignant tumors in the gastrointestinal tract and in extraintestinal tissues. One PJS locus has been mapped to chromosome 19p1...

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Main Authors: Mehenni, H, Gehrig, C, Nezu, J, Oku, A, Shimane, M, Rossier, C, Guex, N, Blouin, J L, Scott, H S, Antonarakis, S E
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377635/
https://ncbi.nlm.nih.gov/pubmed/9837816
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