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Myoclonic Epilepsy, Juvenile
Recent developments in the quest for myoclonic epilepsy genes.
Mutations in EFHC1 cause juvenile myoclonic epilepsy.
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype.
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.
Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.
Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.