Identification of epilepsy genes in human and mouse

Annual Review of Genetics

Volumn 35, Issue , 2001, Pages 567-588

  Meisler, M H ^a   Kearney, J ^a   Ottman, R ^a   Escayg, A ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

Ion channel; Mutation detection; Seizure; Sodium channel

Indexed keywords

4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID A RECEPTOR; ACETYLCHOLINE; CALCIUM CHANNEL; CHOLINERGIC RECEPTOR; GLUTAMATE RECEPTOR; GLUTAMIC ACID; ION CHANNEL; PROTEIN SLC9A; SODIUM CHANNEL; SODIUM PROTON EXCHANGE PROTEIN; UNCLASSIFIED DRUG; VOLTAGE GATED CHANNEL FORMING PROTEIN;

ALLELE; ANIMAL MODEL; COGNITIVE DEFECT; ELECTROPHYSIOLOGY; EPILEPSY; GENE INACTIVATION; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC MARKER; GENETIC MODEL; GENETIC VARIABILITY; GENOME; GENOTYPE; HAPLOTYPE; HETEROZYGOSITY; MASS SCREENING; NERVE EXCITABILITY; PRIORITY JOURNAL; REVIEW; SEIZURE;

ANIMALS; DISEASE MODELS, ANIMAL; EPILEPSY; HUMANS; LINKAGE (GENETICS); MICE; MICE, MUTANT STRAINS; MUTATION; NERVE TISSUE PROTEINS; PHENOTYPE; POTASSIUM CHANNELS; RECEPTORS, CHOLINERGIC; RECEPTORS, NICOTINIC; SODIUM CHANNELS;

ANIMALIA;

EID: 0035676059     PISSN: 00664197     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.genet.35.102401.091142     Document Type: Review

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