Contribution of KCNJ10 gene polymorphisms in childhood epilepsy

Journal of Child Neurology

Volumn 30, Issue 3, 2015, Pages 296-300

  Dai, Alper I ^a   Akcali, Aylin ^a   Koska, Safinur ^a   Oztuzcu, Serdar ^a   Cengiz, Beyhan ^a   Demiryürek, Abdullah T ^a  

^a GAZIANTEP UNIVERSITY   (Turkey)

Author keywords

idiopathic generalized epilepsy; Kir4.1 potassium channel; tonic clonic seizures

Indexed keywords

ETHOSUXIMIDE; GENOMIC DNA; INWARDLY RECTIFYING POTASSIUM CHANNEL; KCNJ10 PROTEIN; LAMOTRIGINE; UNCLASSIFIED DRUG; VALPROIC ACID; KCNJ10 (CHANNEL);

ADOLESCENT; ALLELE; ARTICLE; BENIGN CHILDHOOD EPILEPSY; CHILD; CHILDHOOD ABSENCE EPILEPSY; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENERALIZED EPILEPSY; GENETIC ASSOCIATION; GENOTYPE; GRAND MAL EPILEPSY; HUMAN; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MYOCLONUS EPILEPSY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; TONIC CLONIC SEIZURE; TURK (PEOPLE); ELECTROENCEPHALOGRAPHY; EPILEPSY; GENETIC PREDISPOSITION; GENETICS; INFANT; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; ELECTROENCEPHALOGRAPHY; EPILEPSY; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INFANT; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; POTASSIUM CHANNELS, INWARDLY RECTIFYING;

EID: 84923370487     PISSN: 08830738     EISSN: 17088283     Source Type: Journal    
DOI: 10.1177/0883073814539560     Document Type: Article

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