KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness
Open Access
- 5 February 1999
- journal article
- research article
- Published by Elsevier
- Vol. 96 (3) , 437-446
- https://doi.org/10.1016/s0092-8674(00)80556-5
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- The fundamental and medical impacts of recent progress in research on hereditary hearing lossHuman Molecular Genetics, 1998
- Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairmentNature Genetics, 1998
- The Structure of the Potassium Channel: Molecular Basis of K + Conduction and SelectivityScience, 1998
- How well do we understand the cochlea?Trends in Neurosciences, 1998
- Mutations in the hminK gene cause long QT syndrome and suppress lKs functionNature Genetics, 1997
- Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA geneNature Genetics, 1997
- The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA geneNature Genetics, 1997
- Linkage Analysis of Progressive Hearing Loss in Five Extended Families Maps the DFNA2 Gene to a 1.25-Mb Region on Chromosome 1pGenomics, 1997
- KVLQT1 mutations in three families with familial or sporadic long QT syndromeHuman Molecular Genetics, 1996
- A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probesHistochemistry and Cell Biology, 1993