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2008 | 1 |
2009 | 1 |
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Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies.
Epilepsia. 2011 Jan;52(1):1-9. doi: 10.1111/j.1528-1167.2010.02734.x.
Epilepsia. 2011.
PMID: 21219301
Free PMC article.
Review.
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).
Strug LJ, Clarke T, Chiang T, Chien M, Baskurt Z, Li W, Dorfman R, Bali B, Wirrell E, Kugler SL, Mandelbaum DE, Wolf SM, McGoldrick P, Hardison H, Novotny EJ, Ju J, Greenberg DA, Russo JJ, Pal DK.
Strug LJ, et al.
Eur J Hum Genet. 2009 Sep;17(9):1171-81. doi: 10.1038/ejhg.2008.267. Epub 2009 Jan 28.
Eur J Hum Genet. 2009.
PMID: 19172991
Free PMC article.
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An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder.
Kugler SL, Bali B, Lieberman P, Strug L, Gagnon B, Murphy PL, Clarke T, Greenberg DA, Pal DK.
Kugler SL, et al.
Epilepsia. 2008 Jun;49(6):1086-90. doi: 10.1111/j.1528-1167.2007.01517.x. Epub 2008 Jan 31.
Epilepsia. 2008.
PMID: 18248446
Free PMC article.
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