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ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2023

Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation.

Ikhlass Belhassen et al.PubMed ↗Full text ↗Publisher ↗

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Full record →Abstract, authors, funding and every citing paper · PMID 38406381