Maternally inherited non-syndromic hearing loss is linked with a novel mitochondrial ND6 gene mutation
Author:
Funder
Taizhou Municipal Science and Technology Bureau
Mission on Nano Science and Technology
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11845-023-03484-6.pdf
Reference24 articles.
1. Guan MX (2011) Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity. Mitochondrion 11:237–245
2. Zheng J, Ji Y, Guan MX (2012) Mitochondrial tRNA mutations associated with deafness. Mitochondrion 12:406–413
3. Ding Y, Leng J, Fan F et al (2013) The role of mitochondrial DNA mutations in hearing loss. Biochem Genet 51(7–8):588–602
4. Zhao H, Li R, Wang Q et al (2004) Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am J Hum Genet 74:139–152
5. Yan X, Wang X, Wang Z et al (2011) Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene. J Med Genet 48(10):682–690
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