Genetic Mapping of a Major Susceptibility Locus for Juvenile Myoclonic Epilepsy on Chromosome 15q

The epilepsies are a group of disorders characterised by recurrent seizures caused by episodes of abnormal neuronal hyperexcitability involving the brain. Up to 60 million people are affected worldwide and genetic factors may contribute to the aetiology in up to 40% of patients. The most common huma...

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Veröffentlicht in:	Human molecular genetics 1997-08, Vol.6 (8), p.1329-1334
Hauptverfasser:	Elmslie, Frances V., Rees, Michele, Williamson, Magali P., Kerr, Michael, Kjeldsen, Marianne J., An Pang, Kiang, Sundqvist, Anders, Friis, Mögens L., Chadwick, David, Richens, Alan, Covanis, Athanasios, Santos, Manuela, Arzimanoglou, Alexis, Panayiotopoulos, Chrysostomos P., Curtis, David, Whitehouse, William P., Gardiner, R. Mark
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Chromosome Mapping Chromosomes, Human, Pair 15 Epilepsies, Myoclonic - genetics Genetic Linkage Genetic Predisposition to Disease Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Medical sciences Nervous system (semeiology, syndromes) Neurology Receptors, Nicotinic - genetics
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