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A Missense Mutation (Trp26→Arg) in Exon 3 of the Apolipoprotein CII Gene in a Patient with Apolipoprotein CII Deficiency (Apo CII-Wakayama)

Mendelian DisorderGenetic DisorderApolipoprotein Cii GeneGeneticsPathogenesisInherited Metabolic DiseasePathologyExon 3Apolipoprotein Cii DeficiencyMolecular GeneticsMedical GeneticsDisease Gene IdentificationGenomicsMedicineVariant InterpretationClinical Genetics