Related Articles
Role of dystrophin isoforms and associated proteins in muscular dystrophy (review).
Muscular dystrophy: Experimental animal models and therapeutic approaches (Review)
Compound heterozygous <em>CAPN3</em> variants identified in a family with limb-girdle muscular dystrophy recessive 1
Identification and functional characterization of a novel heterozygous splice‑site mutation in the calpain 3 gene causes rare autosomal dominant limb‑girdle muscular dystrophy
CAPN3: A muscle‑specific calpain with an important role in the pathogenesis of diseases (Review)