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Vol 9, No 3 (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
Kurbatov S.A., Tsygankova P.G., Mollaeva K.Y., Bychkov I.O., Itkis Y.S., Zabnenkova V.V., Umakhanova Z.R., Geybatova L.G., Zakharova E.Y.
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(Rus)
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