X-linked myopathy with excessive autophagy due to a mutation in VMA21 gene: the first case in China.

Neurol Sci

Department of Neurology, The First Affiliated Hospital, Sun Yat-Sen University, 58 2nd Zhongshan Road, Guangzhou, 510080, People's Republic of China.

Published: March 2022

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10072-021-05788-wDOI Listing

Publication Analysis

Top Keywords

x-linked myopathy
4
myopathy excessive
4
excessive autophagy
4
autophagy mutation
4
mutation vma21
4
vma21 gene
4
gene case
4
case china
4
x-linked
1
excessive
1

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!