Genetic testing in the epilepsies-Report of the ILAE Genetics Commission

Erstveröffentlichung
2010
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Authors
Ottman, Ruth
Hirose, Shinichi
Jain, Satish
Lerche, Holger
Lopes-Cendes, Iscia
et al.
Faculties
Medizinische Fakultät
Institutions
UKU. Klinik für Neurologie
Institut für Angewandte Physiologie
Published in
Epilepsia ; 51 (2010), 4. - S. 655-670. - ISSN 0013-9580. - eISSN 1528-1167
Link to publication
https://dx.doi.org/10.1111/j.1528-1167.2009.02429.x
Keywords
Epilepsy; Seizures; Genetics; Genetic testing; SCN1A; IDIOPATHIC GENERALIZED EPILEPSY; SEVERE MYOCLONIC EPILEPSY; CHILDHOOD ABSENCE EPILEPSY; FRONTAL-LOBE EPILEPSY; POTASSIUM CHANNEL GENE; NEONATAL-INFANTILE SEIZURES; DOMINANT PARTIAL EPILEPSY; GLUCOSE-TRANSPORTER GLUT1; NEURONAL SODIUM-CHANNEL; EPISODIC ATAXIA TYPE-1
Dewey Decimal Group
DDC 610 / Medicine & health
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