Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea

Hearing impairment is the most frequent sensory deficit in humans. Deafness genes, which harbor pathogenic mutations that have been identified in families with hereditary hearing loss, are commonly expressed in the auditory end organ or the cochlea and may contribute to normal hearing function, yet...

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Detalles Bibliográficos
Autores principales: Hosoya, Makoto, Fujioka, Masato, Ogawa, Kaoru, Okano, Hideyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768099/
https://www.ncbi.nlm.nih.gov/pubmed/26915689
http://dx.doi.org/10.1038/srep22250

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768099/
https://www.ncbi.nlm.nih.gov/pubmed/26915689
http://dx.doi.org/10.1038/srep22250

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