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Paper Details

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy.
Epilepsia Open
59
2019
NGS gene panel, NGS panel, childhood epilepsy, children, epilepsy, epilepsy-related genes, genes, multi-gene, single-nucleotide variants
Author NameAffiliation
Rebecca Truty
Nila PatilDepartments of Pediatrics and Neurology University of California Los Angeles Los Angeles California.
John J MillichapLurie Children's Hospital and Northwestern University Chicago Illinois.
Edward D Esplin
Edward D Esplin
Robert L Nussbaum
Robert L NussbaumVolunteer Faculty University of California San Francisco San Francisco California.
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Release 1.2