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RGD IDTitleCitationAbstractPubMedPub Date
598120007Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness.Wortmann SB, etal., Nat Genet. 2012 Jun 10;44(7):797-802. doi: 10.1038/ng.2325.Using exome sequencing, we identify SERAC1 mutations as the cause of MEGDEL syndrome, a recessive disorder of dystonia and deafness with Leigh-like syndrome, impaired oxidative phosphorylation and 3-methylglutaconic aciduria. We localized SERAC1226837132012-06-10