Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis.

Lu, Yan; Da, Yu-Wei; Zhang, Yong-Biao; Li, Xin-Gang; Wang, Min; Di, Li; Pang, Mi; Lei, Lin.

Afiliação

Lu Y; Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Da YW; Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Zhang YB; Beijing Advanced Innovation Center for Big Data-Based Precision Medicine, Beihang University, Beijing, China.
Li XG; Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
Wang M; School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia.
Di L; Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Pang M; Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Lei L; Department of Neurology, Zhengzhou University People's Hospital, Zhengzhou, China.

Front Neurosci ; 12: 570, 2018.

Article em En | MEDLINE | ID: mdl-30174583