Germline cytotoxic lymphocytes defective mutations in Chinese patients with lymphoma

Certain patients with lymphoma may harbor mutations in perforin 1 (PRF1), unc-13 homolog D (UNC13D), syntaxin 11 (STX11), STXBP2 (syntaxin binding protein 2) or SH2 domain containing 1A (SH2D1A), which causes functional defects of cytotoxic lymphocytes. Data regarding the association between genetic...

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Detalles Bibliográficos
Autores principales: Chen, Xue, Zhang, Yang, Wang, Fang, Wang, Mangju, Teng, Wen, Lin, Yuehui, Han, Xiangping, Jin, Fangyuan, Xu, Yuanli, Cao, Panxiang, Fang, Jiancheng, Zhu, Ping, Tong, Chunrong, Liu, Hongxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656022/
https://www.ncbi.nlm.nih.gov/pubmed/29113160
http://dx.doi.org/10.3892/ol.2017.6898

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656022/
https://www.ncbi.nlm.nih.gov/pubmed/29113160
http://dx.doi.org/10.3892/ol.2017.6898

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