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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 Faye
Published 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.
Keyphrases
  • case report
  • early onset
  • copy number
  • genome wide
  • fatty acid
  • genome wide identification
  • dna methylation
  • replacement therapy
  • transcription factor
  • smoking cessation