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All references automaticaly matched for cacng3

6. Pubmed Spencer K. et al. Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility. Invest. Ophthalmol. Vis. Sci., 2011 Mar , 52 (1748-54).
5. Pubmed Yalçın O. et al. Genes and molecular mechanisms involved in the epileptogenesis of idiopathic absence epilepsies. , 2011 Dec 27 , ().
4. Pubmed Everett K. et al. Linkage and association analysis of CACNG3 in childhood absence epilepsy. Eur. J. Hum. Genet., 2007 Apr , 15 (463-72).
3. Pubmed Robinson R. et al. Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q. Epilepsy Res., 2002 Feb , 48 (169-79).
2. Pubmed Burgess D. et al. A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene family. Genomics, 2001 Feb 1 , 71 (339-50).
1. Pubmed Burgess D. et al. Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication. Genome Res., 1999 Dec , 9 (1204-13).