Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications
Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications
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Publisher
Ankara: AVES
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Language
English
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Ankara: AVES
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Scope and Contents
Contents
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 ami...
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Research Advances on Deafness Genes Associated with Mitochondrial tRNA-37 Modifications
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10645192
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10645192
Other Identifiers
ISSN
1308-7649
E-ISSN
2148-3817
DOI
10.5152/iao.2023.231107
