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Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2I

Rare DiseasesMendelian DisorderNorwegian PatientsGenetic DisorderGeneticsGenetic EpidemiologyPhenotypic VariabilityBiostatisticsDisease Gene IdentificationPublic HealthMedicineMutation SpectrumClinical Genetics