Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita.

MLA

Weber, Mathilde, et al. “Broadening the Phenotypic Spectrum of TUBA1A Tubulinopathy to Syndromic Arthrogryposis Multiplex Congenita.” American Journal of Medical Genetics. Part A, vol. 188, no. 8, Aug. 2022, pp. 2331–38. EBSCOhost, https://doi.org/10.1002/ajmg.a.62866.

APA

Weber, M., Jaber, D., Encha-Razavi, F., Julien, E., Grevoul-Fesquet, J., Steffann, J., Melki, J., & Martinovic, J. (2022). Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita. American Journal of Medical Genetics. Part A, 188(8), 2331–2338. https://doi.org/10.1002/ajmg.a.62866

Chicago

Weber, Mathilde, Dana Jaber, Ferechte Encha-Razavi, Emmanuel Julien, Julie Grevoul-Fesquet, Julie Steffann, Judith Melki, and Jelena Martinovic. 2022. “Broadening the Phenotypic Spectrum of TUBA1A Tubulinopathy to Syndromic Arthrogryposis Multiplex Congenita.” American Journal of Medical Genetics. Part A 188 (8): 2331–38. doi:10.1002/ajmg.a.62866.