Work

Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss

Year: 2007

Type: article

Study design: Observational Study

Source: Biochemical and Biophysical Research Communications

DOI: 10.1016/j.bbrc.2007.06.171

Authors: Longjin Jin, Aifen Yang, Yi Zhu, Jianyue Zhao, Xinjian Wang, Li Yang, Dongmei Sun, Zhihua Tao, Asami Tsushima, Guomin Wu, Limin Xu, Chongxi Chen, Boquan Yi, Jianxin Cai, Xiaowen Tang, Jindan Wang, Dong Li, Qian Yuan, Zhisu Liao, Jiafu Chen, Zhiyuan Li, Jianxin Lu, Min-Xin Guan

Institutions: Wenzhou Medical University, Cincinnati Children's Hospital Medical Center, First Affiliated Hospital of Wenzhou Medical University, University of Cincinnati

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institute on Deafness and Other Communication Disorders, National Institute of Neurological Disorders and Stroke

Awards: G1481888250, G3168128337, G3662291670, Nuclear modifier genes for maternally inherited deafness, Molecular Mechanism of Aminoglycoside Ototoxicity, Genetic Correction of Maternally Inherited Diseases

OpenAlex ID: W2042982062

FWCI: 2.653

Cites: 38

Cited by: 45

Related to: 10