Recent publication: Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders

It is difficult to identify the genetic causes of specific clinical symptoms of neurodevelopmental disorders due to genetic heterogeneity and overlap of these disorders. Thus, this study identified a module, called MAGI-S, enriched with de novo non-synonymous mutations and can illuminate networks that underlie the epilepsy phenotype.

Chow et al. Genome Medicine 11, 65. Continue reading the article here.

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