Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants

MLA

C. Dejoie, et al. “Implication of the SH3TC2 Gene in Charcot-Marie-Tooth Disease Associated with Deafness and/or Scoliosis: Illustration with Four New Pathogenic Variants.” Journal of the Neurological Sciences, vol. 406, Jan. 2019. EBSCOhost, https://doi.org/10.1016/j.jns.2019.06.027⟩.

APA

C. Dejoie, Justine Lerat, Cyril Goizet, Annick Toutain, M. Rego, P. Beze Beyrie, Corinne Magdelaine, F. Taithe, Jon Andoni Urtizberea, P Calvas, A. Delaubrier, Hubert Journel, Eric Bieth, Brigitte Gilbert-Dussardier, Hélène Dzugan, Laurent Magy, F. Demurger, F. Laffargue, Franck Sturtz, … Anne-Sophie Lia. (2019). Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants. Journal of the Neurological Sciences, 406. https://doi.org/10.1016/j.jns.2019.06.027⟩

Chicago

C. Dejoie, Justine Lerat, Cyril Goizet, Annick Toutain, M. Rego, P. Beze Beyrie, Corinne Magdelaine, et al. 2019. “Implication of the SH3TC2 Gene in Charcot-Marie-Tooth Disease Associated with Deafness and/or Scoliosis: Illustration with Four New Pathogenic Variants.” Journal of the Neurological Sciences 406 (January). doi:10.1016/j.jns.2019.06.027⟩.