Work

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees

Year: 2007

Type: article

Study design: Observational Study

Source: Gene

DOI: 10.1016/j.gene.2007.06.009

Authors: Jianfu Chen, Li Yang, Aifen Yang, Yi Zhu, Jianyue Zhao, Dongmei Sun, Zhihua Tao, Xiaowen Tang, Jindan Wang, Xinjian Wang, Asami Tsushima, Jinshan Lan, Weixing Li, Fangli Wu, Qian Yuan, Jingzhang Ji, Jinbao Feng, Chunli Wu, Zhisu Liao, Zhiyuan Li, John H. Greinwald, Jianxin Lu, Min-Xin Guan

Institutions: Wenzhou Medical University, First Affiliated Hospital of Wenzhou Medical University, Cincinnati Children's Hospital Medical Center, Quzhou City People's Hospital, Zhejiang Provincial People's Hospital, Shaoxing 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: green

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: W2038521731

FWCI: 2.341

Cites: 46

Cited by: 45

Related to: 10