Genetic epilepsies

European Journal of Paediatric Neurology

Volumn 15, Issue 1, 2011, Pages 88-89

  Striano, Pasquale ^a   Zara, Federico ^a  

^a UNIVERSITY OF GENOA   (Italy)

Author keywords

Classification; Epilepsy; Genetics

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR ALPHA1; 4 AMINOBUTYRIC ACID A RECEPTOR GAMMA2; CYCLIN DEPENDENT KINASE LIKE 5; NICOTINIC RECEPTOR ALPHA4; NICOTINIC RECEPTOR BETA2; POTASSIUM CHANNEL KCNQ2; POTASSIUM CHANNEL KCNQ3; PROTEIN; PROTOCADHERIN; SODIUM CHANNEL; SODIUM CHANNEL NAV1.1; SODIUM CHANNEL NAV1.2; SYNTAXIN BINDING PROTEIN 1; UNCLASSIFIED DRUG; VOLTAGE GATED SODIUM CHANNEL ALPHA1;

BENIGN FAMILIAL INFANTILE SEIZURE; BENIGN FAMILIAL NEONATAL INFANTILE SEIZURE; EARLY ONSET ABSENCE EPILEPSY; EPILEPSY; HEREDITARY EPILEPSY; MYOCLONUS EPILEPSY; NOTE; OHTHARA SYNDROME; PRIORITY JOURNAL; SEVERE MYOCLONIC EPILEPSY IN INFANCY; X LINKED INFANTILE SPASM; ADOLESCENT; ARTICLE; CHILD; CLASSIFICATION; GENETIC PREDISPOSITION; GENETICS; HUMAN; INFANT; METABOLIC ENCEPHALOPATHY; MUTATION; NEWBORN; PRESCHOOL CHILD;

ADOLESCENT; BRAIN DISEASES, METABOLIC, INBORN; CHILD; CHILD, PRESCHOOL; EPILEPSY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; INFANT, NEWBORN; MUTATION;

EID: 84855523747     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2010.05.004     Document Type: Article

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