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Atypical cases of hearing loss in patients with the mitochondrial variant m.1555A>G of the <i>MT-RNR1</i> gene in the Republic of Buryatia

In the previous study, we found a high prevalence of the m.1555A&gt;G variant of the MT-RNR1 gene, which causes mitochondrial hearing loss (OMIM 561000) among deaf patients living in the Baikal Lake region. In this regard, in the present study, a genotype-phenotypic analysis of the hearing function...

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Principais autores: F. M. Teryutin, T. V. Borisova, A. M. Cherdonova, G. P. Romanov, V. G. Pshennikova, A. V. Solovyov, S. A. Fedorova, N. A. Barashkov
Format: Artigo
Jezik:Russo
Izdano: Yakut Science Center of Complex Medical Problems 2025-06-01
Serija:Якутский медицинский журнал
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Online dostop:https://ymj.elpub.ru/jour/article/view/768
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