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Coursimault J, Guerrot AM, Morrow MM, et al. MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects. Hum Genet. 2021;141(1):65-80doi: 10.1007/s00439-021-02383-z.
Coursimault, J., Guerrot, A. M., Morrow, M. M., Schramm, C., Zamora, F. M., Shanmugham, A., Liu, S., Zou, F., Bilan, F., Le Guyader, G., Bruel, A. L., Denommé-Pichon, A. S., Faivre, L., Tran Mau-Them, F., Tessarech, M., Colin, E., El Chehadeh, S., Gérard, B., Schaefer, E., Cogne, B., Isidor, B., Nizon, M., Doummar, D., Valence, S., Héron, D., Keren, B., Mignot, C., Coutton, C., Devillard, F., Alaix, A. S., Amiel, J., Colleaux, L., Munnich, A., Poirier, K., Rio, M., Rondeau, S., Barcia, G., Callewaert, B., Dheedene, A., Kumps, C., Vergult, S., Menten, B., Chung, W. K., Hernan, R., Larson, A., Nori, K., Stewart, S., Wheless, J., Kresge, C., Pletcher, B. A., Caumes, R., Smol, T., Sigaudy, S., Coubes, C., Helm, M., Smith, R., Morrison, J., Wheeler, P. G., Kritzer, A., Jouret, G., Afenjar, A., Deleuze, J. F., Olaso, R., Boland, A., Poitou, C., Frebourg, T., Houdayer, C., Saugier-Veber, P., Nicolas, G., & Lecoquierre, F. (2022). MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects. Human genetics, 141(1), 65-80. https://doi.org/10.1007/s00439-021-02383-z
Coursimault, Juliette, et al. "MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects." Human genetics vol. 141,1 (2022): 65-80. doi: https://doi.org/10.1007/s00439-021-02383-z
Coursimault J, Guerrot AM, Morrow MM, Schramm C, Zamora FM, Shanmugham A, Liu S, Zou F, Bilan F, Le Guyader G, Bruel AL, Denommé-Pichon AS, Faivre L, Tran Mau-Them F, Tessarech M, Colin E, El Chehadeh S, Gérard B, Schaefer E, Cogne B, Isidor B, Nizon M, Doummar D, Valence S, Héron D, Keren B, Mignot C, Coutton C, Devillard F, Alaix AS, Amiel J, Colleaux L, Munnich A, Poirier K, Rio M, Rondeau S, Barcia G, Callewaert B, Dheedene A, Kumps C, Vergult S, Menten B, Chung WK, Hernan R, Larson A, Nori K, Stewart S, Wheless J, Kresge C, Pletcher BA, Caumes R, Smol T, Sigaudy S, Coubes C, Helm M, Smith R, Morrison J, Wheeler PG, Kritzer A, Jouret G, Afenjar A, Deleuze JF, Olaso R, Boland A, Poitou C, Frebourg T, Houdayer C, Saugier-Veber P, Nicolas G, Lecoquierre F. MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects. Hum Genet. 2022 Jan;141(1):65-80. doi: 10.1007/s00439-021-02383-z. Epub 2021 Nov 08. PMID: 34748075.
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