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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Med Sci Monit
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: International Scientific Literature, Inc. 2016
Soggetti:
Clinical Research
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi