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Identification of a novel mutation in the ANGPTL3 gene in two families diagnosed of familial hypobetalipoproteinemia without APOB mutation

Allelic VariantGenetic DisorderFamilial HypobetalipoproteinemiaGeneticsInherited Metabolic DiseaseGenetic EpidemiologyDisease Gene IdentificationAngptl3 GeneMedicineApob MutationClinical Genetics