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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. http://access.bl.uk/ark:/81055/vdc_100135562805.0x000035