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Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion

Crossref DOI link: https://doi.org/10.1007/s12041-022-01417-3

Published Online: 2023-01-24

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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