Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q

Epilepsy Research - Tập 88 - Trang 65-75 - 2010
Auli Sirén1,2, Anne Polvi2, Lyne Chahine3, Malgorzata Labuda4, Sarah Bourgoin5, Anna-Kaisa Anttonen2, Maria Kousi2, Kari Hirvonen6, Kalle O.J. Simola7, Eva Andermann8, Asta Laiho9, Juhani Soini10, Matti Koivikko1, Reijo Laaksonen11, Massimo Pandolfo3,5, Anna-Elina Lehesjoki2
1Department of Pediatrics, Tampere University Hospital, Teiskontie 35, 33521 Tampere, Finland
2Folkhälsan Institute of Genetics, Department of Medical Genetics and Neuroscience Center, Haartmaninkatu 8, 00290 Helsinki, Finland
3Laboratory of Experimental Neurology, Department of Neurology, Erasme Hospital, Free University of Brussels, Route de Lennik 808, B-1070, Brussels, Belgium
4Research Center Ste-Justine Hospital, Montreal, 3175 Cote-Ste-Catherine, Montreal, QC, H3T 1C5, Canada
5Centre de Recherche, Centre Hospitalier de l’Université de Montréal, 2099 Alexander de Seve, Montreal, QC, H2L 4W5, Canada
6Regional Medical Imaging Centre, Pirkanmaa Hospital District, Tampere University Hospital, Teiskontie 35, 33521 Tampere, Finland
7Genetics Clinic, Department of Pediatrics, Tampere University Hospital, Teiskontie 35, 33521 Tampere, Finland
8Neurogenetics Unit, Montreal Neurological Hospital, Department of Neurology and Neurosurgery and Human Genetics, McGill University, 3801 University Street, Montreal, QC, H3A 2B4, Canada
9Finnish DNA Microarray Centre, Turku Centre for Biotechnology, Tykistökatu 6, 20521 Turku, Finland
10Turku Centre for Biotechnology, University of Turku and Åbo Akademi, Tykistökatu 6, 20521 Turku, Finland
11Science Center, Tampere University Hospital, Biokatu 12, 33521 Tampere, Finland

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