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The Homozygous Pathogenic CAPN3 Variant Identified Using Whole-exome Sequencing in Iranian Family With Limb-girdle Muscular Dystrophy Recessive 1

Crossref DOI link: https://doi.org/10.32598/bcn.2024.5978.1

Published Online: 2024-11-01

Update policy: https://doi.org/10.32598/nsp.crossmark-policy

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