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Benvenga S, Lakshmanan M, Trimarchi F
Most clinicians can manage this with a short follow-up and simple lab checks
NDUFA5 is a part of complex I of the ETC and its mutations may contribute to ASD [86]
As the name suggests, MHADD involves the deficiency of medium-chain 3-hydroxyacyl-CoA dehydrogenase, an enzyme that processes MCFAs and SCFAs
[DOI] [PubMed] [Google Scholar] 186.Fox JG, Wang TC
