Chelban, V., Wiethoff, S., Fabian‐Jessing, B. K., Haridy, N. A., Khan, A., Efthymiou, S., . . . Houlden, H. (2018). Genotype‐phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14. Mov Disord.
استشهاد بنمط شيكاغوChelban, Viorica, et al. "Genotype‐phenotype Correlations, Dystonia and Disease Progression in Spinocerebellar Ataxia Type 14." Mov Disord 2018.
MLA استشهادChelban, Viorica, et al. "Genotype‐phenotype Correlations, Dystonia and Disease Progression in Spinocerebellar Ataxia Type 14." Mov Disord 2018.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.