EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities.

MLA

Shaw, Marie, et al. “EXOME REPORT: Novel Mutation in ATP6V1B2 Segregating with Autosomal Dominant Epilepsy, Intellectual Disability and Mild Gingival and Nail Abnormalities.” European Journal of Medical Genetics, vol. 63, no. 4, Apr. 2020, p. 103799. EBSCOhost, https://doi.org/10.1016/j.ejmg.2019.103799.

APA

Shaw, M., Winczewska-Wiktor, A., Badura-Stronka, M., Koirala, S., Gardner, A., Kuszel, Ł., Kowal, P., Steinborn, B., Starczewska, M., Garry, S., Scheffer, I. E., Berkovic, S. F., & Gecz, J. (2020). EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities. European Journal of Medical Genetics, 63(4), 103799. https://doi.org/10.1016/j.ejmg.2019.103799

Chicago

Shaw, Marie, Anna Winczewska-Wiktor, Magdalena Badura-Stronka, Sunita Koirala, Alison Gardner, Łukasz Kuszel, Piotr Kowal, et al. 2020. “EXOME REPORT: Novel Mutation in ATP6V1B2 Segregating with Autosomal Dominant Epilepsy, Intellectual Disability and Mild Gingival and Nail Abnormalities.” European Journal of Medical Genetics 63 (4): 103799. doi:10.1016/j.ejmg.2019.103799.