Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome

BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease characterized by gastrointestinal hamartomatous polyps and mucocutaneous melanin spots. Germline mutation of the serine/threonine kinase 11 (STK11) gene are responsible for PJS. In this study, we investigated the...

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Detalles Bibliográficos
Autores principales: Huang, Zhiheng, Miao, Shijian, Wang, Lin, Zhang, Ping, Wu, Bingbing, Wu, Jie, Huang, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659168/
https://www.ncbi.nlm.nih.gov/pubmed/26607058
http://dx.doi.org/10.1186/s12876-015-0397-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659168/
https://www.ncbi.nlm.nih.gov/pubmed/26607058
http://dx.doi.org/10.1186/s12876-015-0397-9

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