LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures

Annals of Neurology

Volumn 52, Issue 3, 2002, Pages 364-367

  Gu, Wenli ^a   Brodtkorb, Eylert ^b   Steinlein, Ortrud K ^a  

^a UNIVERSITY HOSPITAL BONN   (Germany)

^b TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE;

APHASIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 10Q; CLINICAL ARTICLE; CLINICAL FEATURE; GENE ISOLATION; GENETIC ASSOCIATION; GENETIC LINKAGE; GLIOMA; HUMAN; LGI1 GENE; MISSENSE MUTATION; NORWAY; PRIORITY JOURNAL; SEIZURE; TEMPORAL LOBE EPILEPSY;

APHASIA; DNA MUTATIONAL ANALYSIS; EPILEPSY, TEMPORAL LOBE; FAMILY HEALTH; FEMALE; HUMANS; MALE; MUTATION, MISSENSE; NORWAY; PEDIGREE; PROTEINS;

EID: 0036712759     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10280     Document Type: Article

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