机构:[1]The Fourth School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China,[2]Department of Neurology, Hangzhou First People’s Hospital, Hangzhou, China,[3]Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, SAR China,[4]Department of Hematology, Affiliated Hangzhou First People’s Hospital, Zhejiang University, Hangzhou, China,[5]Department of Cardiology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, China,[6]Department of Neurology, First Affiliated Hospital of Kunming Medical University, Kunming Medical University, Kunming, China内科科室神经内科昆明医科大学附属第一医院
Yunnan provincial medical reserve talents (H-2017032),
Zhejiang Traditional Chinese Medicine Science and Technology
Plan (2021ZQ074), and Zhejiang Provincial Medical and health
Science and Technology Plan (2021KY849).
第一作者机构:[1]The Fourth School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China,[2]Department of Neurology, Hangzhou First People’s Hospital, Hangzhou, China,
共同第一作者:
通讯作者:
通讯机构:[1]The Fourth School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China,[2]Department of Neurology, Hangzhou First People’s Hospital, Hangzhou, China,
推荐引用方式(GB/T 7714):
Wenqing Xia,Zhumei Ni,Zheng Zhang,et al.Case Report: A Boy From a Consanguineous Family Diagnosed With Congenital Muscular Dystrophy Caused by Integrin Alpha 7 (ITGA7) Mutation.[J].FRONTIERS IN GENETICS.2021,12:doi:10.3389/fgene.2021.706823.
APA:
Wenqing Xia,Zhumei Ni,Zheng Zhang,Hongfei Sang,Huifang Liu...&Xiaoguang Lei.(2021).Case Report: A Boy From a Consanguineous Family Diagnosed With Congenital Muscular Dystrophy Caused by Integrin Alpha 7 (ITGA7) Mutation..FRONTIERS IN GENETICS,12,
MLA:
Wenqing Xia,et al."Case Report: A Boy From a Consanguineous Family Diagnosed With Congenital Muscular Dystrophy Caused by Integrin Alpha 7 (ITGA7) Mutation.".FRONTIERS IN GENETICS 12.(2021)