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Peutz-Jeghers syndrome without STK11 mutation may correlate with less severe clinical manifestations in Chinese patients

BACKGROUND: Peutz-Jeghers syndrome (PJS) is an autosomal dominant genetic disease with skin mucosal pigment spots and gastrointestinal (GI) multiple hamartoma polyps as clinical characteristics. At present, it is considered that the germline mutation of STK11 gene is the genetic cause of PJS. Howeve...

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Detalles Bibliográficos
Autores principales:	Jiang, Li-Xin, Chen, Yu-Rui, Xu, Zu-Xin, Zhang, Yu-Hui, Zhang, Zhi, Yu, Peng-Fei, Dong, Zhi-Wei, Yang, Hai-Rui, Gu, Guo-Li
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Baishideng Publishing Group Inc 2023
Materias:	Clinical Trials Study
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292148/ https://www.ncbi.nlm.nih.gov/pubmed/37377590 http://dx.doi.org/10.3748/wjg.v29.i21.3302

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