A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene.
Robin ChautardCécile Laroche-RaynaudAnne-Sophie LiaPauline ChazelasPaco DerouaultFranck SturtzYasser BaajAlice Veauville-MerlliéCécile AcquavivaFrédéric FavreauPierre-Antoine FayePublished in: BMC medical genomics (2020)
This case report describes new pathogenic variations of the ETFA gene. These compound heterozygous mutations induce the production of altered proteins, leading to a mild form of MADD.