Clinical, Imaging, Morphologic, and Molecular Features of X-linked VMA21-related Myopathy in Two Unrelated Brazilian Families
Overview
Authors
Affiliations
Bardhan M, Polavarapu K, Baskar D, Preethish-Kumar V, Vengalil S, Nashi S Glob Med Genet. 2024; 11(2):167-174.
PMID: 38736558 PMC: 11087142. DOI: 10.1055/s-0044-1786815.
Phenotype variability and natural history of X-linked myopathy with excessive autophagy.
Fernandez-Eulate G, Alfieri G, Spinazzi M, Ackermann-Bonan I, Duval F, Sole G J Neurol. 2024; 271(7):4008-4018.
PMID: 38517523 DOI: 10.1007/s00415-024-12298-0.
Pegat A, Streichenberger N, Lacoste N, Hermier M, Menassa R, Coudert L Genes (Basel). 2022; 13(12).
PMID: 36553512 PMC: 9777698. DOI: 10.3390/genes13122245.