Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families

Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families

Mitochondrial transfer RNA mutation is one of the most important causes of hereditary hearing loss in humans. Mitochondrial transfer RNASer (UCN) gene is another hot spot for mutations associated with non-syndromic hearing loss, besides the 12S ribosomal RNA gene. In this study, we assessed the clin...

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Bibliographic Details
Main Authors: Dejun Zhang, Jie Wu, Yongyi Yuan, Xiaohong Li, Xue Gao, Dongyang Kang, Xin Zhang, Sha-sha Huang, Pu Dai
Format: Article
Language:English
Published: Elsevier 2024-03-01
Series:Heliyon
Subjects:
Hearing loss
Mitochondria
Transfer RNA
Non-syndromic
Transfer RNASer(UCN)
Online Access:http://www.sciencedirect.com/science/article/pii/S240584402403072X

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