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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Detalles Bibliográficos
Autores principales: Wang, Zhiqing, Chen, Yulan, Wu, Baoping, Zheng, Haoxuan, He, Jiman, Jiang, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297525/
https://www.ncbi.nlm.nih.gov/pubmed/22168747
http://dx.doi.org/10.1186/1471-2350-12-161

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297525/
https://www.ncbi.nlm.nih.gov/pubmed/22168747
http://dx.doi.org/10.1186/1471-2350-12-161

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