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Browsing by Author Muhle, H.

Full Text	Issue Date	Title	Author(s)
	2010	Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.	Mefford, H.C.; Muhle, H.; Ostertag, P.; Spiczak, S. von; Buysse, K., et al
	2010	Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.	Reutlinger, C.; Helbig, I.; Gawelczyk, B.; Subero, J.I.; Tonnies, H., et al