Fig. 2From: A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese familySequence analysis of ETFDH gene mutation in proband and her parents. The heterozygous variant c.1399G > C in exon 11 was identified in proband (a) and her mother (c); the variant c.623_626 del in exon 6 was identified in proband (b) and her father (d)Back to article page