机构:[1]Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China,神经内科首都医科大学宣武医院[2]Beijing Advanced Innovation Center for Big Data-Based Precision Medicine, Beihang University, Beijing, China,[3]Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China,[4]School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia,[5]Department of Neurology, Zhengzhou University People’s Hospital, Zhengzhou, China
第一作者机构:[1]Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China,
通讯作者:
通讯机构:[1]Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China,[2]Beijing Advanced Innovation Center for Big Data-Based Precision Medicine, Beihang University, Beijing, China,
推荐引用方式(GB/T 7714):
Yan Lu,Yu-Wei Da,Yong-Biao Zhang,et al.Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis (vol 12, 329, 2018)[J].FRONTIERS IN NEUROSCIENCE.2018,12(AUG):570.doi:10.3389/fnins.2018.00570.
APA:
Yan Lu,Yu-Wei Da,Yong-Biao Zhang,Xin-Gang Li,Min Wang...&Lin Lei.(2018).Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis (vol 12, 329, 2018).FRONTIERS IN NEUROSCIENCE,12,(AUG)
MLA:
Yan Lu,et al."Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis (vol 12, 329, 2018)".FRONTIERS IN NEUROSCIENCE 12..AUG(2018):570