Luca Bello
Università degli Studi di Padova
9 papers found
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Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy
Download from doi.orgAblation of collagen VI leads to the release of platelets with altered function
Download from doi.orgClinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy
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