HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice

Hereditary hearing loss is a clinically and genetically heterogeneous disorder. More than 80 genes have been implicated to date, and with the advent of targeted genomic enrichment and massively parallel sequencing (TGE+MPS) the rate of novel deafness-gene identification has accelerated. Here we repo...

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Detalles Bibliográficos
Autores principales: Azaiez, Hela, Decker, Amanda R., Booth, Kevin T., Simpson, Allen C., Shearer, A. Eliot, Huygen, Patrick L. M., Bu, Fengxiao, Hildebrand, Michael S., Ranum, Paul T., Shibata, Seiji B., Turner, Ann, Zhang, Yuzhou, Kimberling, William J., Cornell, Robert A., Smith, Richard J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376867/
https://www.ncbi.nlm.nih.gov/pubmed/25816005
http://dx.doi.org/10.1371/journal.pgen.1005137

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376867/
https://www.ncbi.nlm.nih.gov/pubmed/25816005
http://dx.doi.org/10.1371/journal.pgen.1005137

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