Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN/A gene

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Bibliographic Details
Published inEpilepsia (Copenhagen) Vol. 51; no. 12; pp. 2474 - 2477
Main Authors GUERRINI, Renzo, CELLINI, Elena, MEI, Davide, METITIERI, Tiziana, PETRELLI, Cristina, PUCATTI, Daniela, MARINI, Carla, ZAMPONI, Nelia
Format Journal Article
LanguageEnglish
Published Malden, MA Wiley-Blackwell 2010
Subjects
Anticonvulsants. Antiepileptics. Antiparkinson agents
Biological and medical sciences
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Medical sciences
Nervous system (semeiology, syndromes)
Neurology
Neuropharmacology
Pharmacology. Drug treatments
Nervous system diseases
Epilepsy
Intrafamilial heterogeneity
Cerebral disorder
Heterogeneity
Phenotype
Convulsion
MLPA
Central nervous system disease
Dravet syndrome
SCN9A
Deletion
Neurological disorder
Seizures
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ISSN:0013-9580
1528-1167