Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation

Authors: de Vries, Boukje1; Stam, Anine H.2; Kirkpatrick, Martin3; Vanmolkot, Kaate R.J.1; Koenderink, Jan B.4; van den Heuvel, Jeroen J.M.W.4; Stunnenberg, Bas4; Goudie, David5; Shetty, Jay3; Jain, Vivek3; van Vark, Judith1; Terwindt, Gisela M.2; Frants, Rune R.1; Haan, Joost; van den Maagdenberg, Arn M.J.M.; Ferrari, Michel D.2

Source: Epilepsia, Volume 50, Number 11, November 2009 , pp. 2503-2504(2)

Publisher: Blackwell Publishing

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Document Type: Research article

DOI: 10.1111/j.1528-1167.2009.02186.x

Affiliations: 1: Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands 2: Department of Neurology, Leiden University Medical Centre, The Netherlands 3: Department of Paediatrics, Tayside Children's Hospital, Dundee, United Kingdom 4: Department of Pharmacology and Toxicology, Nijmegen Centre for Molecular Life Sciences,Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands 5: Department of Clinical Genetics, Tayside Children's Hospital, Dundee, United Kingdom

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