Four new families with autosomal dominant partial epilepsy with auditory features: Clinical description and linkage to chromosome 10q24

Epilepsia

Volumn 43, Issue 1, 2002, Pages 60-67

  Winawer, Melodie R ^a,c   Boneschi, Filippo Martinelli ^a,c   Barker Cummings, Christie ^a,c   Lee, Joseph H ^a,c   Liu, Jianjun ^b   Mekios, Constantine ^b,c   Gilliam, T Conrad ^b,c,d   Pedley, Timothy A ^c   Hauser, W Allen ^a,c   Ottman, Ruth ^a,c,d  

^a Taub Institute for Research on Alzheimer's Disease and the Aging Brain and the Gertrude H Sergievsky Center   (United States)

^b New York State Psychiatric Institute ^*  (United States)

^c Och Spine at New York Presbyterian Hospitals   (United States)

^d NEW YORK STATE PSYCHIATRIC INSTITUTE   (United States)

Author keywords

Auditory; Epidemiology; Epilepsy; Focal; Genetics; Linkage; Phenotype

Indexed keywords

MICROSATELLITE DNA;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 10Q; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER SYSTEM; CONTROLLED STUDY; FAMILIAL DISEASE; FOCAL EPILEPSY; GENE LOCATION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENOTYPE; HEARING DISORDER; HUMAN; IDIOPATHIC DISEASE; LINKAGE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SCORING SYSTEM; TEMPORAL LOBE EPILEPSY;

ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 10; EPILEPSIES, PARTIAL; FAMILY HEALTH; FEMALE; GENES, DOMINANT; HALLUCINATIONS; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; PHENOTYPE;

EID: 0036192726     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1528-1157.2002.45001.x     Document Type: Article

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