Fromer2014

Genes affected by de novo mutations in schizophrenia, filtered for genes occurring in the initial Epi4K cohort and annotated for all other studies that have used trio exome sequencing on a large scale in neurodevelopmental disorders. In green, de novo mutations in controls or unaffected sibs are shown. SCN2A clearly stands out as a gene that is found in a broad range of phenotypes.

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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