Kurbatov, S. A., Tsygankova, P. G., Mollaeva, K. Y., Bychkov, I. O., Itkis, Y. S., Zabnenkova, V. V., . . . Zakharova, E. Y. (2019). Infantile and early childhood onset of mitochondrial myopathy due to mutations in the TK2 gene with a phenotype of spinal muscular atrophy 5q: The first cases in Russia. Nervno-myshechnye bolezni, 9(3), 67-76. https://doi.org/10.17650/2222-8721-2019-9-3-57-76
Citácia podle Chicago (17th ed.)Kurbatov, S. A., P. G. Tsygankova, K. Yu Mollaeva, I. O. Bychkov, Yu. S. Itkis, V. V. Zabnenkova, Z. R. Umakhanova, L. G. Geybatova, a E. Yu Zakharova. "Infantile and Early Childhood Onset of Mitochondrial Myopathy Due to Mutations in the TK2 Gene with a Phenotype of Spinal Muscular Atrophy 5q: The First Cases in Russia." Nervno-myshechnye Bolezni 9, no. 3 (2019): 67-76. https://doi.org/10.17650/2222-8721-2019-9-3-57-76.
Citácia podľa MLA (8th ed.)Kurbatov, S. A., et al. "Infantile and Early Childhood Onset of Mitochondrial Myopathy Due to Mutations in the TK2 Gene with a Phenotype of Spinal Muscular Atrophy 5q: The First Cases in Russia." Nervno-myshechnye Bolezni, vol. 9, no. 3, 2019, pp. 67-76, https://doi.org/10.17650/2222-8721-2019-9-3-57-76.