KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference43 articles.
1. KvLQT1 and IsK (minK) proteins associate to form the IKs cardiac potassium current;Barhanin;Nature,1996
2. A potassium channel mutation in neonatal human epilepsy;Biervert;Science,1998
3. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family;Charlier;Nat. Genet.,1998
4. Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias;Chouabe;EMBO J.,1997
5. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families;Coucke;N. Engl. J. Med.,1994
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1. The potassium channel subunit KV1.8 (Kcna10) is essential for the distinctive outwardly rectifying conductances of type I and II vestibular hair cells;2024-09-04
2. The potassium channel subunit KV1.8 (Kcna10) is essential for the distinctive outwardly rectifying conductances of type I and II vestibular hair cells;2024-09-04
3. Neurocardiac pathologies associated with potassium channelopathies;Epilepsia;2024-08
4. Selective inhibition of A-fiber-mediated excitatory transmission underlies the analgesic effects of KCNQ channel opening in the spinal dorsal horn;Neuropharmacology;2024-08
5. Contemporary directions in the therapy of sensory hearing loss;Otolaryngologia Polska;2024-07-25
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