Human Genome Epidemiology Literature Finder
Records 1 - 1 (of 1 Records) |
Query Trace: ARHGEF15[original query] |
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Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses. Journal of medical genetics 2018 5 55 (9): 607-616. Addis Laura, Sproviero William, Thomas Sanjeev V, Caraballo Roberto H, Newhouse Stephen J, Gomez Kumudini, Hughes Elaine, Kinali Maria, McCormick David, Hannan Siobhan, Cossu Silvia, Taylor Jacqueline, Akman Cigdem I, Wolf Steven M, Mandelbaum David E, Gupta Rajesh, van der Spek Rick A, Pruna Dario, Pal Deb |
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- Page last updated:Apr 22, 2024
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