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Paper Details

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet
185
2010
16p13, Patients, deletions, epilepsy, epilepsy disorders, epilepsy syndromes, genomic regions, haploinsufficiency, homologous chromosome, homologous interval, idiopathic generalized epilepsy, locus-specific deletions, mental retardation, non-, patients, recessive mutations, schizophrenia, sporadic epilepsy syndromes
Chromosomes, Human, Pair 16, Disease Susceptibility, Epilepsy, Humans, Mutation, Nucleic Acid Hybridization, Sequence Deletion, Syndrome
Author NameAffiliation
Erin L HeinzenCenter for Human Genome Variation, Duke University
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