Work

Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASer(UCN) gene in a Japanese family

Year: 2005

Type: article

Study design: Observational Study

Source: Biochemical and Biophysical Research Communications

DOI: 10.1016/j.bbrc.2004.12.140

Authors: Ronghua Li, Kotaro Ishikawa, Jian-Hong Deng, Selena Heman-Ackah, Yuya Tamagawa, Li Yang, Yidong Bai, Keiichi Ichimura, Min-Xin Guan

Institutions: Cincinnati Children's Hospital Medical Center, Jichi Medical University, The University of Texas at San Antonio Health Science Center, Wenzhou Medical University, University of Cincinnati, University of Cincinnati Medical Center

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: American Heart Association, United Mitochondrial Disease Foundation, National Institutes of Health, National Institute on Deafness and Other Communication Disorders

Awards: G3609014522, G4277256131, G4913640580, G5227788746, Biochemical Basis of Maternally Inherited Deafness, G6755582793

OpenAlex ID: W2071621045

FWCI: 3.648

Cites: 34

Cited by: 54

Related to: 10