Yulya Fomicheva
2PUBLICATIONS
7CO-AUTHORS

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Publications (2)
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|Jun 03, 2025
[Phenotypic heterogeneity of Charcot-Marie-Tooth type 2A disease associated with the c.1091G>C missense mutation (p.Arg364Pro) in the MFN2 gene].T M Alekseeva, A I Vlasenko, V S Demeshenok
|Jul 26, 2024
The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis.Olga Irtyuga, Rostislav Skitchenko, Mary Babakekhyan
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