Publication | Open Access

Hyperhomocysteinemia Due to Methionine Synthase Deficiency, cblG: Structure of the MTR Gene, Genotype Diversity, and Recognition of a Common Mutation, P1173L

Mendelian DisorderBiochemistryCommon MutationMedicineGeneticsInherited Metabolic DiseaseNatural SciencesHuman PolymorphismMolecular BiologyGenetic DisorderMolecular GeneticsMtr GeneMethionine Synthase DeficiencyMolecular Medicine