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Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

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Year: 2014
Type: article
Source: Neurobiology of Disease
DOI: 10.1016/j.nbd.2014.02.002
Authors: Taku Ito, Xiangming Li, Kiyoto Kurima, Byung Yoon Choi, Philine Wangemann, Andrew J. Griffith
Institutions: National Institutes of Health, National Institute on Deafness and Other Communication Disorders, Kansas State University
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: University of Kansas, National Institute for Health and Care Research, National Institutes of Health, National Institutes of Natural Sciences, National Institute on Deafness and Other Communication Disorders, National Center for Research Resources
Awards: G2943335313, Fluid transport in inner ear development, G5116215330, Epithelial Function in Health and Disease, G6529111306, G7637750969, Identification of Genes Causing Syndromic And Nonsyndromic Hearing Impairment, Identification of Genes Causing Syndromic and Nonsyndromic Hearing Impairment, Molecular Analysis Of Human Hereditary Deafness
OpenAlex ID: W2026230551
FWCI: 2.259
Cites: 71
Cited by: 51
Related to: 10
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