Publication | Open Access

Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey

Agl GeneAllelic VariantGenetic DisorderMedicineGeneticsMolecular AnalysisGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene IdentificationGenomicsMolecular DiagnosticsLysosomal Storage Disease