Evidence of linkage to chromosome 5p13.2‐q11.1 in a large inbred family with genetic generalized epilepsy - Kinay, Demet; Oliver, Karen L.; Tüzün, Erdem; Damiano, John A.; Ulusoy, Canan; Andermann, Eva; Hildebrand, Michael S.; Bahlo, Melanie; Berkovic, Samuel F. (Epilepsia (Copenhagen), 2018)
Keywords: Adolescent; Child; Chromosome 5; Chromosomes, Human, Pair 5 - genetics; Consanguinity; EEG; Epilepsy; Epilepsy, Generalized - genetics; Eyelid; Family Health; Female; Firing pattern; Genetic Linkage; genetics; Haplotypes; HCN1; Heredity; Humans; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - genetics; Inbreeding; Ion channels (cyclic nucleotide-gated); juvenile myoclonic epilepsy; linkage analysis; Male; Phenotypes; Phenotyping; Polymorphism, Single Nucleotide - genetics; Seizures; Turkey; Young Adult; Turkey; genetics; linkage analysis; consanguinity; juvenile myoclonic epilepsy; HCN1