Identification of potential modifier genes in Chinese patients with Wilson disease

The mutations in modifier genes may contribute to some inherited diseases including Wilson disease (WD). This study was designed to identify potential modifier genes that contribute to WD. A total of 10 WD patients with single or no heterozygous ATP7B mutations were recruited for whole-exome sequenc...

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Detalles Bibliográficos
Autores principales: Zhou, Donghu, Jia, Siyu, Yi, Liping, Wu, Zhen, Song, Yi, Zhang, Bei, Li, Yanmeng, Yang, Xiaoxi, Xu, Anjian, Li, Xiaojin, Zhang, Wei, Duan, Weijia, Li, Zhenkun, Qi, Saiping, Chen, Zhibin, Ouyang, Qin, Jia, Jidong, Huang, Jian, Ou, Xiaojuan, You, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9154322/
https://www.ncbi.nlm.nih.gov/pubmed/35357466
http://dx.doi.org/10.1093/mtomcs/mfac024

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