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.
Chicago Style CitationZagnoli-Vieira, Guido, Francesco Bruni, Kyle Thompson, Langping He, Sarah Walker, Arjan P.M de Brouwer, Robert Taylor, Dmitriy Niyazov, and Keith W. Caldecott. "Confirming TDP2 Mutation in Spinocerebellar Ataxia Autosomal Recessive 23 (SCAR23)." Neurol Genet 2018.
MLA CitationZagnoli-Vieira, Guido, et al. "Confirming TDP2 Mutation in Spinocerebellar Ataxia Autosomal Recessive 23 (SCAR23)." Neurol Genet 2018.
Warning: These citations may not always be 100% accurate.