Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice

Autosomal-dominant sensorineural hearing loss is genetically heterogeneous, with a phenotype closely resembling presbycusis, the most common sensory defect associated with aging in humans. We have identified SLC17A8, which encodes the vesicular glutamate transporter-3 (VGLUT3), as the gene responsib...

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Hauptverfasser: Ruel, Jérôme, Emery, Sarah, Nouvian, Régis, Bersot, Tiphaine, Amilhon, Bénédicte, Van Rybroek, Jana M., Rebillard, Guy, Lenoir, Marc, Eybalin, Michel, Delprat, Benjamin, Sivakumaran, Theru A., Giros, Bruno, El Mestikawy, Salah, Moser, Tobias, Smith, Richard J.H., Lesperance, Marci M., Puel, Jean-Luc
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2008
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2495073/
https://ncbi.nlm.nih.gov/pubmed/18674745
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2008.07.008
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