TRPML3 mutations cause impaired mechano-electrical transduction and depolarization by an inward-rectifier cation current in auditory hair cells of varitint-waddler mice.
J Physiol
; 586(22): 5403-18, 2008 Nov 15.
Article
em En
| MEDLINE
| ID: mdl-18801844
ABSTRACT
TRPML3 (mucolipin-3) belongs to one of the transient-receptor-potential (TRP) ion channel families. Mutations in the Trpml3 gene cause disorganization of the stereociliary hair bundle, structural aberrations in outer and inner hair cells and stria vascularis defects, leading to deafness in the varitint-waddler (Va) mouse. Here we refined the stereociliary localization of TRPML3 and investigated cochlear hair cell function in varitint-waddler (Va(J)) mice carrying the TRPML3
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Base de dados:
MEDLINE
Assunto principal:
Canais de Cátion TRPM
/
Células Ciliadas Auditivas
/
Mutação
Idioma:
En
Ano de publicação:
2008
Tipo de documento:
Article