Autosomal dominant partial epilepsy with auditory features: Description of a new family

Epilepsia

Volumn 41, Issue 8, 2000, Pages 967-970

  Michelucci, R ^a   Passarelli, D ^a   Pitzalis, S ^b   Dal Corso, G ^c   Tassinari, C A ^a   Nobile, C ^b  

^a UNIVERSITY OF BOLOGNA   (Italy)

^b CNR   (Italy)

^c UNIVERSITY OF PADOVA   (Italy)

Author keywords

Auditory features; Chromosome 10q24; Familial lateral temporal lobe epilepsy; Familial temporal lobe epilepsy; Genetic analysis

Indexed keywords

ADULT; AGED; ALLELE; ARTICLE; AUDIOGENIC SEIZURE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHROMOSOME 10Q; FEMALE; FOCAL EPILEPSY; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; PRIORITY JOURNAL; TEMPORAL LOBE; TONIC CLONIC SEIZURE;

ADOLESCENT; ADULT; AUDITORY PERCEPTION; CHILD; CHROMOSOMES, HUMAN, PAIR 10; EPILEPSY, TEMPORAL LOBE; EPILEPSY, TONIC-CLONIC; FAMILY; FEMALE; GENETIC MARKERS; GENOTYPE; HUMANS; ITALY; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; PEDIGREE; SOUND; TEMPORAL LOBE;

EID: 0033869040     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1528-1157.2000.tb00280.x     Document Type: Article

References (10)

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4. Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2
5. Autosomal dominant rolandic epilepsy and speech dyspraxia: A new syndrome with anticipation
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7. An integrated physical and genetic map spanning chromosome band 10q24
8. Comprehensive genetic map of the human genome based on 5264 microsatellites
9. Familial temporal lobe epilepsy: A clinically heterogeneous syndrome
10. MRI abnormalities in familial temporal lobe epilepsy