APA (7th ed.) Citation

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

Chicago Style (17th ed.) Citation

Kurbatov, S. A., P. G. Tsygankova, K. Yu Mollaeva, I. O. Bychkov, Yu. S. Itkis, V. V. Zabnenkova, Z. R. Umakhanova, L. G. Geybatova, and 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.

MLA (9th ed.) Citation

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.