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Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations

Mexican PopulationMendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyHuman PolymorphismGenetic VariationSteroid 21-Hydroxylase DeficiencyMolecular Genetic AnalysisVariant InterpretationClinical Genetics