KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: Expansion of the functional and mutation spectrum

Brain

Volumn 126, Issue 12, 2003, Pages 2726-2737

  Singh, Nanda A ^a   Westenskow, Peter ^b   Charlier, Carole ^d   Pappas, Chris ^a   Leslie, Jonathan ^a   Dillon, Jessica ^b   Anderson, V Elving ^c   Sanguinetti, Michael C ^b   Leppert, Mark F ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF UTAH   (United States)

^c UNIVERSITY OF MINNESOTA   (United States)

^d UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

Generalized seizures; KCNQ2; KCNQ3; Neonatal epilepsy; Voltage gated potassium channel

Indexed keywords

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BENIGN CHILDHOOD EPILEPSY; CLINICAL ARTICLE; CONTROLLED STUDY; GENE; GENE DELETION; GENE EXPRESSION SYSTEM; GENE FUNCTION; GENE MUTATION; HUMAN; MOLECULAR CLONING; MULTIGENE FAMILY; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; PHENOTYPE; POTASSIUM CHANNEL SUBFAMILY Q MEMBER 2 GENE; POTASSIUM CHANNEL SUBFAMILY Q MEMBER 3 GENE; PRIORITY JOURNAL; ROLANDIC EPILEPSY; SEIZURE; XENOPUS;

EID: 0344012023     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/awg286     Document Type: Article

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