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XB-ANAT-490
Papers associated with tail (and kcnc1)
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Encephalopathies with KCNC1 variants: genotype-phenotype-functional correlations., Cameron JM., Ann Clin Transl Neurol. July 1, 2019; 6 (7): 1263-1272.  |
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A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy., Muona M., Nat Genet. January 1, 2015; 47 (1): 39-46.  |
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Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1., Aidery P., Gene. December 10, 2012; 511 (1): 26-33.  |
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Novel, potent inhibitors of human Kv1.5 K+ channels and ultrarapidly activating delayed rectifier potassium current., Lagrutta A., J Pharmacol Exp Ther. June 1, 2006; 317 (3): 1054-63. |
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Role of transmembrane segment S5 on gating of voltage-dependent K+ channels., Shieh CC., J Gen Physiol. June 1, 1997; 109 (6): 767-78.  |
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