Research output

Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability

Research output: Contribution to journalArticleAcademicpeer-review

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    Research areas

  • genetic diagnosis, learning disability, next generation sequencing, seizures, DE-NOVO MUTATIONS, GENETICS, ENCEPHALOPATHY, EPIDEMIOLOGY, LAMOTRIGINE, GENOMICS, CHILDREN, PEOPLE, GRIN2A, PAPER
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Details

Original languageEnglish
Pages (from-to)155-164
Number of pages10
JournalEpilepsia
Volume60
Issue number1
DOIs
Publication statusPublished - Jan 2019