DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Heinzen EL, Radtke RA, Urban TJ , et al.
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet 2010;
86 (5) 707-718
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