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Presynaptic Ca2+ channels: a functional patchwork.
Reid CA, Bekkers JM, Clements JD. Reid CA, et al. Trends Neurosci. 2003 Dec;26(12):683-7. doi: 10.1016/j.tins.2003.10.003. Trends Neurosci. 2003. PMID: 14624853 Review.
A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy.
Powell KL, Cain SM, Ng C, Sirdesai S, David LS, Kyi M, Garcia E, Tyson JR, Reid CA, Bahlo M, Foote SJ, Snutch TP, O'Brien TJ. Powell KL, et al. Among authors: reid ca. J Neurosci. 2009 Jan 14;29(2):371-80. doi: 10.1523/JNEUROSCI.5295-08.2009. J Neurosci. 2009. PMID: 19144837 Free PMC article.
Mechanisms of human inherited epilepsies.
Reid CA, Berkovic SF, Petrou S. Reid CA, et al. Prog Neurobiol. 2009 Jan 12;87(1):41-57. doi: 10.1016/j.pneurobio.2008.09.016. Epub 2008 Oct 5. Prog Neurobiol. 2009. PMID: 18952142 Review.
206 results