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)
The most recent citing publications are shown below. View all 19 publications that cite this research output on Dimensions.
Article in Experimental and Therapeutic Medicine (January 2024)
Article in Annals of Indian Academy of Neurology (June 2023)
Article in Applied Radiology (March 2023)