Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: A European case

European Journal of Paediatric Neurology

Volumn 17, Issue 3, 2013, Pages 308-310

  Fister, Petja ^a   Soltirovska Salamon, Aneta ^a   Debeljak, Marusa ^a   Paro Panjan, Darja ^a  

^a UNIVERSITY CHILDREN S HOSPITAL   (Slovenia)

Author keywords

Convulsions; Epilepsy; Family; Mutation; Newborn

Indexed keywords

GENOMIC DNA; PHENOBARBITAL;

ANAMNESIS; ARTICLE; BENIGN CHILDHOOD EPILEPSY; CASE REPORT; CHILD; CLINICAL FEATURE; EXON; FAMILY HISTORY; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; INFANT; NEWBORN; POLYMERASE CHAIN REACTION; POTASSIUM CHANNEL KCNQ3 GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE;

EPILEPSY, BENIGN NEONATAL; EXONS; FEMALE; GENOTYPE; HUMANS; INFANT, NEWBORN; KCNQ3 POTASSIUM CHANNEL; MUTATION, MISSENSE; SLOVENIA;

EID: 84875868732     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2012.10.007     Document Type: Article

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