Lopez, E., Berenguer, M., Tingaud-Sequeira, A., Marlin, S., Toutain, A., Denoyelle, F., Picard, A., Charron, S., Mathieu, G., de Belvalet, H., Arveiler, B., Babin, P.J., Lacombe, D., Rooryck, C. (2016) Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS.. Journal of Medical Genetics. 53(11):752-760

Lopez, E., Berenguer, M., Tingaud-Sequeira, A., Marlin, S., Toutain, A., Denoyelle, F., Picard, A., Charron, S., Mathieu, G., de Belvalet, H., Arveiler, B., Babin, P.J., Lacombe, D., Rooryck, C. (2016) Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS.. Journal of Medical Genetics. 53(11):752-760