Analysis of the Spectrum of the mtDNA Haplogroups in Patients with Hearing Loss Carrying the Likely Pathogenic Ultra-Rare m.1494C>T Variant in the MT-RNR1 Gene › Research Explorer

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Analysis of the Spectrum of the mtDNA Haplogroups in Patients with Hearing Loss Carrying the Likely Pathogenic Ultra-Rare m.1494C>T Variant in the MT-RNR1 Gene

Research output: Contribution to journal › Article › peer-review

Section of Molecular Biology and Biotechnology

DOI

https://doi.org/10.1134/S1022795425700504
Final published version

T. V. Borisova
A. M. Cherdonova
V. G. Pshennikova
F. M. Teryutin
I. V. Morozov
A. A. Bondar
O. A. Baturina
M. R. Kabilov
G. P. Romanov
A. V. Solovyev
S. A. Fedorova
N. A. Barashkov

Original language	English
Article number	9
Pages (from-to)	974-986
Number of pages	13
Journal	Russian Journal of Genetics
Volume	61
Issue number	8
DOIs	https://doi.org/10.1134/S1022795425700504
Publication status	Published - Aug 2025

OECD FOS+WOS

1.06.KM GENETICS & HEREDITY

Research areas

Baikal Lake region, MT-RNR1 gene, aminoglycoside-induced deafness, haplogroup A*, m.1494C>T, mtDNA

ID: 68992293