FAMILIAL AND SPORADIC 15Q13.3 MICRODELETIONS IN IDIOPATHIC GENERALIZED EPILEPSY: A MODEL FOR DISORDERS WITH COMPLEX INHERITANCE

被引：0
|
作者：
Mulley, John C. [1 ,2 ]
Dibbens, L. M. [1 ,2 ]
Mullen, S. [3 ,4 ]
Helbig, I. [5 ,6 ,10 ]
Mefford, H. C. [7 ,8 ]
Bayly, M. A. [1 ]
Bellows, S. [3 ,4 ]
Leu, C. [9 ,10 ]
Trucks, H. [9 ,10 ]
Obermeier, T. [5 ,6 ,10 ]
Wittig, M. [5 ,6 ,10 ]
Franke, A. [5 ,6 ,10 ]
Caglayan, H. [10 ,11 ]
Yapica, Z. [10 ,11 ]
Sander, T. [5 ,6 ,10 ]
Eichler, E. E. [7 ,8 ]
Scheffer, I. E. [3 ,4 ]
Berkovic, S. F. [3 ,4 ]
机构：
[1] Womens & Childrens Hosp, Adelaide, SA, Australia
[2] Univ Adelaide, Sch Paediat & Reprod Hlth, Adelaide, SA, Australia
[3] Univ Melbourne, Epilepsy Res Ctr, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[5] Univ Med Ctr Schleswig Holstein, Dept Neuropediat, Kiel, Germany
[6] Univ Med Ctr Schleswig Holstein, Inst Clin Mol Biol, Kiel, Germany
[7] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[8] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[9] Univ Cologne, Cologne Ctr Genom, Cologne, Germany
[10] EPICURE, Kiel, Germany
[11] Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
来源：
EPILEPSIA | 2009年 / 50卷
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中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
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页码：151 / 152
页数：2
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