MYT1

Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS
Estelle Lopez, Marie Berenguer, Angèle Tingaud-Sequeira, Sandrine Marlin, Annick Toutain, Françoise Denoyelle, Arnaud Picard, Sabine Charron, Guilaine Mathieu, Harmony de Belvalet, Benoit Arveiler, Patrick J Babin, Didier Lacombe, Caroline Rooryck

Journal of Medical Genetics Nov 2016, 53 (11) 752-760; DOI: 10.1136/jmedgenet-2016-103774

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MYT1