Ion channels in health and disease. 83rd Boehringer Ingelheim Fonds International Titisee Conference
- PMID: 11463739
- PMCID: PMC1083959
- DOI: 10.1093/embo-reports/kve145
Ion channels in health and disease. 83rd Boehringer Ingelheim Fonds International Titisee Conference
References
-
- Browne D.L., Gancher, S.T., Nutt, J.G., Brunt, E.R., Smith, E.A., Kramer, P. and Litt, M. (1994) Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nature Genet., 8, 136–140. - PubMed
-
- Bulman D.E., Scoggan, K.A., van Oene, M.D., Nicolle, M.W., Hahn, A.F., Tollar, L.L. and Ebers, G.C. (1999) A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology, 53, 1932–1936. - PubMed
-
- Chang S.S. et al. (1996) Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nature Genet., 12, 248–253. - PubMed
-
- Charlier C., Singh, N.A., Ryan, S.G., Lewis, T.B., Reus, B.E., Leach, R.J. and Leppert, M.A. (1998) Pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nature Genet., 18, 53–55. - PubMed
-
- Fisher S.E., Black, G.C., Lloyd, S.E., Hatchwell, E., Wrong, O., Thakker, R.V. and Craig, I.W. (1994) Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent’s disease (an X-linked hereditary nephrolithiasis). Hum. Mol. Genet., 3, 2053–2059. - PubMed
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