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Mutation of TBCE causes hypoparathyroidism– retardation–dysmorphism and autosomal recessive Kenny–Caffey syndrome

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseasePathologyHypoparathyroidism– Retardation–dysmorphismMolecular GeneticsMedical GeneticsMedicineGenetic BasisClinical Genetics