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Paper Details

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Am J Hum Genet
83
2012
IGE, Idiopathic generalized epilepsy, absence epilepsy, copy-number variants, epilepsy, epilepsy disorders, exome sequences, idiopathic generalized epilepsy, juvenile myoclonic epilepsy, rare variants, risk factors, single variants, single-nucleotide variant
Author NameAffiliation
Erin L HeinzenCenter for Human Genome Variation, Duke University School of Medicine
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Release 1.2