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Article

Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications.

The journal of international advanced otology - 1 Oct 2023

Bian Panpan, Chai Jing, Xu Baicheng

Abstract excerpt

As the most common cause of speech disorders, the etiological study of deafness is important for the diagnosis and treatment of deafness. The mitochondrial genome has gradually become a hotspot for deafness genetic research. Mitochondria are the core organelles of energy and material metabolism in eukaryotic cells. Human mitochondria contain 20 amino acids, except for tRNALeu and tRNASer, which have 2...

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Identifiers

PMID: 37789629
DOI: 10.5152/iao.2023.231107
PMCID: PMC10645192

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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