Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

Nature Genetics

Volumn 30, Issue 3, 2002, Pages 335-341

  Kalachikov, Sergey ^a   Evgrafov, Oleg ^a   Ross, Barbara ^a   Winawer, Melodie ^b,c   Barker Cummings, Christie ^b,c   Boneschi, Filippo Martinelli ^b,c   Choi, Chang ^c   Morozov, Pavel ^a   Das, Kamna ^a   Teplitskaya, Elita ^a   Yu, Andrew ^a   Cayanis, Eftihia ^a   Penchaszadeh, Graciela ^a,c,d   Kottmann, Andreas H ^c   Pedley, Timothy A ^c   Hauser, W Allen ^b,c   Ottman, Ruth ^b,c,d   Gilliam, T Conrad ^a,c  

^a Columbia University ^*  (United States)

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

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

^d NEW YORK STATE PSYCHIATRIC INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; FOCAL EPILEPSY; GENE EXPRESSION; GENE IDENTIFICATION; GENE INACTIVATION; GENE MUTATION; GLIOMA; HUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SEIZURE; TEMPORAL LOBE EPILEPSY;

ANIMALS; AUDITORY DISEASES, CENTRAL; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; DNA; EPILEPSY; FEMALE; GENES, DOMINANT; GENOTYPE; HUMANS; MALE; MUTATION; PEDIGREE; PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 18544376557     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng832     Document Type: Article

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