APA način citiranja

Huang, L., Chardon, J. W., Carter, M. T., Friend, K. L., Dudding, T. E., Schwartzentruber, J., . . . Boycott, K. M. (2012). Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. BioMed Central.

Čikaški stil citiranja

Huang, Lijia, et al. Missense Mutations in ITPR1 Cause Autosomal Dominant Congenital Nonprogressive Spinocerebellar Ataxia. BioMed Central, 2012.

MLA način citiranja

Huang, Lijia, et al. Missense Mutations in ITPR1 Cause Autosomal Dominant Congenital Nonprogressive Spinocerebellar Ataxia. BioMed Central, 2012.