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CAPN3 protein
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Comparative gene expression profiling between cultured and tissue human skeletal muscle
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Missense mutation of c.635 T > C in CAPN3 impairs muscle injury repair in a Limb-Girdel Muscular Dys…
CAPN3 c.1746-20C>G variant is hypomorphic for LGMD R1 calpain 3-related.
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-…
Mutational Spectrum of CAPN3 with Genotype-Phenotype Correlations in Limb Girdle Muscular Dystrophy …
Developing fluorescence sensor probe to capture activated muscle-specific calpain-3 (CAPN3) in livin…
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