Heinzen2012_2

Study design of the Heinzen study. Exome sequencing was performed in a screening cohort, followed by large-scale genotyping of almost 4000 risk variants in a second, independent cohort.

Ingo Helbig

Child Neurology Fellow and epilepsy genetics researcher at the Children’s Hospital of Philadelphia (CHOP), USA and Department of Neuropediatrics, Kiel, Germany

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