DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Carvill GL, Heavin SB, Yendle SC , et al.
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Nat Genet 2013;
45 (7) 825-830
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