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All references automaticaly matched for Kcnab2


4. Pubmed Portero V. et al. Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome. J Am Heart Assoc, 2016 , 5 ().
3. Pubmed Ling C. et al. A pilot genome-scale profiling of DNA methylation in sporadic pituitary macroadenomas: association with tumor invasion and histopathological subtype. PLoS ONE, 2014 , 9 (e96178).
2. Pubmed Christophersen I. et al. Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation. Eur. Heart J., 2013 May , 34 (1517-25).
1. Pubmed Perkowski J. et al. Deletion of the mouse homolog of KCNAB2, a gene linked to monosomy 1p36, results in associative memory impairments and amygdala hyperexcitability. J. Neurosci., 2011 Jan 5 , 31 (46-54).