A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus-And prevalence of variants in patients with epilepsy

American Journal of Human Genetics

Volumn 68, Issue 4, 2001, Pages 866-873

  Escayg, Andrew ^a   Heils, Armin ^b   Macdonald, Bryan T ^a   Haug, Karsten ^c   Sander, Thomas ^d   Meisler, Miriam H ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b UNIVERSITY HOSPITAL BONN   (Germany)

^c UNIVERSITY OF BONN   (Germany)

^d CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN SCN1A; PROTEIN SUBUNIT; SODIUM CHANNEL; UNCLASSIFIED DRUG;

ABSENCE; ALLELE; ARTICLE; CHROMOSOME 2Q; CONTROLLED STUDY; FEBRILE CONVULSION; GENE FREQUENCY; GENE MUTATION; GENERALIZED EPILEPSY; GENERALIZED EPILEPSY WITH FEBRILE SEIZURE PLUS; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MYOCLONUS EPILEPSY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0035071143     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/319524     Document Type: Article

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