Differential Expression of KCNQ4 in Inner Hair Cells and Sensory Neurons Is the Basis of Progressive High-Frequency Hearing Loss

Human KCNQ4 mutations known as DFNA2 cause non-syndromic, autosomal-dominant, progressive high-frequency hearing loss in which the cellular and molecular basis is unclear. We provide immunofluorescence data showing that Kcnq4 expression in the adult cochlea has both longitudinal (base to apex) and r...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Beisel, Kirk W., Rocha-Sanchez, Sonia M., Morris, Ken A., Nie, Liping, Feng, Feng, Kachar, Bechara, Yamoah, Ebenezer N., Fritzsch, Bernd
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2005
Assuntos:
Cellular/Molecular
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6725753/
https://ncbi.nlm.nih.gov/pubmed/16207888
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2110-05.2005
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