Publication | Closed Access

Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis—The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes

Developmental BiologySignal TransductionMolecular PhysiologyGenetic DisorderMendelian DisorderGeneticsInherited Metabolic DiseasePathologyCongenital DisorderMolecular GeneticsBiosynthesis—the PhenotypePgap2 GenesMedicine