Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome

BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease caused by a germline mutation in the STK11 gene. It is characterized by mucocutaneous pigmentation, gastrointestinal hamartomatous polyps, and cancer predisposition. AIMS: We aimed to summarize the main clinical...

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Detalles Bibliográficos
Autores principales: Wu, Bo-Da, Wang, Yong-Jun, Fan, Liang-Liang, Huang, Hui, Zhou, Peng, Yang, Mei, Shi, Xiao-Liu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240661/
https://www.ncbi.nlm.nih.gov/pubmed/32462036
http://dx.doi.org/10.1155/2020/9159315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240661/
https://www.ncbi.nlm.nih.gov/pubmed/32462036
http://dx.doi.org/10.1155/2020/9159315

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