Identification of novel pathogenic variants of Calpain-3 gene in limb girdle muscular dystrophy R1
Article in Orphanet Journal of Rare Diseases (April 2024)
The most recent citing publications are shown below. View all 3 publications that cite this research output on Dimensions.
Identification and functional characterization of a novel heterozygous splice‑site mutation in the calpain 3 gene causes rare autosomal dominant limb‑girdle muscular dystrophy
Article in Experimental and Therapeutic Medicine (January 2024)
Annexins and Membrane Repair Dysfunctions in Muscular Dystrophies
Article in International Journal of Molecular Sciences (May 2021)