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    Srour, M., Hamdan, F. F., Schwartzentruber, J. A., Patry, L., Ospina, L. H., Shevell, M. I., Désilets, V., Dobrzeniecka, S., Mathonnet, G., Lemyre, E., Massicotte, C., Labuda, D., Amrom, D., Andermann, E., Sébire, G., Maranda, B., Consortium, F. C., Rouleau, G. A., Majewski, J., & Michaud, J. L. (2012). mutations in TMEM231 cause Joubert syndrome in French Canadians. Journal of medical genetics, 49(10), 636–641. http://access.bl.uk/ark:/81055/vdc_100137793714.0x000044