KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss
about
Distinct roles of molecular chaperones HSP90α and HSP90β in the biogenesis of KCNQ4 channelsGenetics of hearing loss: focus on DFNA2.Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairmentImpaired surface expression and conductance of the KCNQ4 channel lead to sensorineural hearing lossRestoration of ion channel function in deafness-causing KCNQ4 mutants by synthetic channel openers.Hair Cell Transduction, Tuning, and Synaptic Transmission in the Mammalian Cochlea.Downregulation of KCNQ4 by Janus kinase 2.Cyclodextrins and Iatrogenic Hearing Loss: New Drugs with Significant Risk.
P2860
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P2860
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on October 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss
@en
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.
@nl
type
label
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss
@en
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.
@nl
prefLabel
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss
@en
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss.
@nl
P2860
P1476
KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss
@en
P2093
Liping Nie
P2860
P304
P356
10.1097/MOO.0B013E32830F4AA3
P577
2008-10-01T00:00:00Z