N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita-Reference-Cited by-同舟云学术

N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita

Published:2017-10-15 Issue:22 Volume:595 Page:6837-6850
ISSN:0022-3751
Container-title:The Journal of Physiology
language:en
Short-container-title:J Physiol

Author:

Ke Qing¹,Ye Jia²,Tang Siyang²,Wang Jin³,Luo Benyan¹,Ji Fang¹,Zhang Xu⁴,Yu Ye³,Cheng Xiaoyang⁵,Li Yuezhou²^ORCID

Affiliation:

1. Department of Neurology, The First Affiliated Hospital; Zhejiang University School of Medicine; Hangzhou Zhejiang China

2. Department of Physiology, Institute of Neuroscience, Key Laboratory of Medical Neurobiology of Ministry of Health of China, Zhejiang Province Key Laboratory of Tissue Engineering and Regenerative Medicine; Zhejiang University School of Medicine; Hangzhou Zhejiang China

3. Institute of Medical Sciences and Department of Pharmacology; Shanghai Jiao Tong University School of Medicine; Shanghai China

4. Bejing Epigen Medical Institute; Beijing China

5. Department of Anatomy, Histology and Embryology; Shanghai Jiao Tong University School of Medicine; Shanghai China

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Natural Science Foundation of Zhejiang Province

Health bureau foundation of zhejiang province

National 863 Program of China

Fundamental Research Funds for the Central Universities

Chinese Ministry of Education Project 111 Program

Publisher