Loss of the potassium channel β-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome

Epilepsia

Volumn 42, Issue 9, 2001, Pages 1103-1111

  Heilstedt, Heidi A ^a   Burgess, Daniel L ^a   Anderson, Anne E ^a   Chedrawi, Aziza ^a   Tharp, Barry ^a   Lee, Olivia ^a   Kashork, Catherine D ^a   Starkey, David E ^a   Wu, Yuan Qing ^a   Noebels, Jeffrey L ^a   Shaffer, Lisa G ^a,b   Shapira, Stuart K ^a,c  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b Health Science Center ^*  (United States)

^c UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

Chromosome 1p36; Deletion; Epilepsy; Potassium channel

Indexed keywords

GENE PRODUCT; POTASSIUM CHANNEL; PROTEIN KCNAB2; PROTEIN SUBUNIT; UNCLASSIFIED DRUG;

ARTICLE; CHILD; CHROMOSOME 1P; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; EPILEPSY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; SEIZURE SUSCEPTIBILITY;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; CRANIOFACIAL ABNORMALITIES; ELECTROENCEPHALOGRAPHY; EPILEPSY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MENTAL RETARDATION; MUTATION; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 0034785511     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1528-1157.2001.08801.x     Document Type: Article

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