Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS. Lopez E, Berenguer M, Tingaud-Sequeira A, Marlin S, Toutain A, Denoyelle F, Picard A, Charron S, Mathieu G, de Belvalet H, et al. J Med Genet. 2016 Jun 29. PMID: 27358179. Abstract CommentRecommendBookmarkWatch