A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients

BACKGROUND: Peutz-Jeghers syndrome (PJS) is caused by mutations in the tumor suppressor gene, STK11, and is characterized by gastrointestinal hamartomas, melanin spots on the lips, and an increased risk of developing cancer. METHODS: Blood samples were collected from two unrelated Chinese PJS famili...

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Bibliografiske detaljer
Main Authors: Wang, Zhiqing, Chen, Yulan, Wu, Baoping, Zheng, Haoxuan, He, Jiman, Jiang, Bo
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2011
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3297525/
https://ncbi.nlm.nih.gov/pubmed/22168747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-161
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