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Article

Advances in Genetics of Juvenile Myoclonic Epilepsies

1 May 2007

Abstract excerpt

One by one, mutation-containing mendelian genes that cause monogenic juvenile myoclonic epilepsies (JME) and single nucleotide polymorphisms (SNP)-susceptibility alleles that increase risks for nonmendelian complex JME should fall to the power of molecular genetics. Of 15 chromosome loci, 3 mendelian genes (alpha1-subunit of the GABA(A) receptor [GABRA1], chloride channel 2 gene [CLCN2], and Myoclonin1/EFHC1) and...

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PMID: 17520076
DOI: 10.1111/j.1535-7511.2007.00171.x

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