Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
Open Access
- 14 May 2010
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 86 (5), 707-718
- https://doi.org/10.1016/j.ajhg.2010.03.018
Abstract
No abstract availableKeywords
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