Showing 1 - 3 results of 3 for search 'I. O. Bychkov', query time: 0.03s Refine Results
  1. 1
    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

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

    Published 2019-11-01
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  2. 2
    Clinical case of Mitochondrial DNA Depletion

    Clinical case of Mitochondrial DNA Depletion by A. V. Degtyareva, E. V. Stepanova, Yu. S. Itkis, E. I. Dorofeeva, M. V. Narogan, L. V. Ushakova, A. A. Puchkova, V. G. Bychenko, P. G. Tsygankova, T. D. Krylova, I. O. Bychkov

    Published 2017-11-01
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  3. 3
    Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12

    Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12 by I.O. Panchuk, O.V. Grigorieva, E.V. Kondrateva, E.V. Kurshakova, VYu. Tabakov, I.O. Bychkov, EYu. Zakharova, M.D. Orlova, E.S. Voronina, V.O. Pozhitnova, A.V. Lavrov, S.A. Smirnikhina, S.I. Kutsev

    Published 2023-09-01
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