Case report: Novel ETFDH compound heterozygous mutations identified in a patient with late-onset glutaric aciduria type II

RT @FrontNeurol: New Research: Case report: Novel ETFDH compound heterozygous mutations identified in a patient with late-onset glutaric ac…

Case report: Novel ETFDH compound heterozygous mutations identified in a patient with late-onset glutaric aciduria type II https://t.co/xkDtyUk7Z9 https://t.co/q9PKvJrVpk

New Research: Case report: Novel ETFDH compound heterozygous mutations identified in a patient with late-onset glutaric aciduria type II: Glutaric aciduria type II (GA II) is an autosomal recessive metabolic disorder of fatty acid, amino acid,… https://t.c