致编辑的信：根据疾病阶段和修饰因素，与线粒体DNA相关的听力损失可由多种线粒体DNA突变引起。 - Suppr

Suppr

超能文献

Letter to the Editor: Depending on the Disease Stage and Modifying Factors, mtDNA-Associated Hearing Loss Can Occur With Many mtDNA Mutations.

作者信息

Finsterer Josef

机构信息

Neurology & Neurophysiology Center, Vienna, Austria.

出版信息

J Korean Med Sci. 2024 Jan 22;39(3):e41. doi: 10.3346/jkms.2024.39.e41.

DOI:10.3346/jkms.2024.39.e41

PMID:38258368

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10803210/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c7d/10803210/2b76d081e69b/jkms-39-e41-g001.jpg

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本文引用的文献

Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.

J Korean Med Sci. 2023 Dec 11;38(48):e355. doi: 10.3346/jkms.2023.38.e355.

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Nature. 2024 Jan;625(7993):92-100. doi: 10.1038/s41586-023-06045-0. Epub 2023 Dec 6.

The Role of Primary Mitochondrial Disorders in Hearing Impairment: An Overview.

Medicina (Kaunas). 2023 Mar 19;59(3):608. doi: 10.3390/medicina59030608.

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Genome Res. 2022 Mar;32(3):569-582. doi: 10.1101/gr.276013.121. Epub 2022 Jan 24.

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