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Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia.
Kistol D, Tsygankova P, Krylova T, Bychkov I, Itkis Y, Nikolaeva E, Mikhailova S, Sumina M, Pechatnikova N, Kurbatov S, Bostanova F, Migiaev O, Zakharova E. Kistol D, et al. Among authors: tsygankova p. Int J Mol Sci. 2023 Jan 13;24(2):1597. doi: 10.3390/ijms24021597. Int J Mol Sci. 2023. PMID: 36675121 Free PMC article.
Gene symbol: WFS1. Disease: Wolfram syndrome.
Tsygankova P, Zakharova EY, Stepina DP. Tsygankova P, et al. Hum Genet. 2008 Feb;123(1):113. Hum Genet. 2008. PMID: 18386376 No abstract available.
Previously Unclassified Mutation of mtDNA m.3472T>C: Evidence of Pathogenicity in Leber's Hereditary Optic Neuropathy.
Sheremet NL, Nevinitsyna TA, Zhorzholadze NV, Ronzina IA, Itkis YS, Krylova TD, Tsygankova PG, Malakhova VA, Zakharova EY, Tokarchuk AV, Panteleeva AA, Karger EM, Lyamzaev KG, Avetisov SE. Sheremet NL, et al. Among authors: tsygankova pg. Biochemistry (Mosc). 2016 Jul;81(7):748-54. doi: 10.1134/S0006297916070117. Biochemistry (Mosc). 2016. PMID: 27449621 Free article.
27 results