Genetic Screening and Analysis of LKB1 Gene in Chinese Patients with Peutz-Jeghers Syndrome

BACKGROUND: Peutz-Jeghers syndrome (PJS) is an autosomal dominant genetic disease. It severely decreases patient quality of life and leads elevated cancer risk. Germline mutation of LKB1 is the leading cause of familial PJS. MATERIAL/METHODS: To characterize the germline mutation of LKB1 gene in Chi...

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Detalles Bibliográficos
Publicado en:Med Sci Monit
Main Authors: Chen, Chunyan, Zhang, Xiaomei, Wang, Deqiang, Wang, Fangyu, Pan, Jian, Wang, Zhenkai, Liu, Chang, Wu, Lin, Lu, Heng, Li, Nan, Wei, Juan, Shi, Hui, Wan, Haijun, Zhu, Ming, Chen, Senqing, Zhou, Yun, Zhou, Xin, Yang, Liu, Liu, Jiong
Formato: Artigo
Idioma:Inglês
Publicado: International Scientific Literature, Inc. 2016
Assuntos:
Clinical Research
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5070620/
https://ncbi.nlm.nih.gov/pubmed/27721366
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/MSM.897498
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