Neurological diseases caused by ion-channel mutations
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference73 articles.
1. Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice;Cox;Cell,1997
2. Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment;Xia;Nat Genet,1998
3. Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness;Karet;Nat Genet,1999
4. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness;Kubisch;Cell,1999
5. Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter;Delpire;Nat Genet,1999
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