Zagnoli-Vieira, G., Bruni, F., Thompson, K., He, L., Walker, S., de Brouwer, A. P., . . . Caldecott, K. W. (2018). Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23). Neurol Genet.
استشهاد بنمط شيكاغوZagnoli-Vieira, Guido, Francesco Bruni, Kyle Thompson, Langping He, Sarah Walker, Arjan P.M de Brouwer, Robert Taylor, Dmitriy Niyazov, و Keith W. Caldecott. "Confirming TDP2 Mutation in Spinocerebellar Ataxia Autosomal Recessive 23 (SCAR23)." Neurol Genet 2018.
MLA استشهادZagnoli-Vieira, Guido, et al. "Confirming TDP2 Mutation in Spinocerebellar Ataxia Autosomal Recessive 23 (SCAR23)." Neurol Genet 2018.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.