Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders

Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders

Abstract Background Neurodevelopmental disorders (NDDs) such as autism spectrum disorder, intellectual disability, developmental disability, and epilepsy are characterized by abnormal brain development that may affect cognition, learning, behavior, and motor skills. High co-occurrence (comorbidity)...

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Bibliographic Details
Main Authors: Julie Chow, Matthew Jensen, Hajar Amini, Farhad Hormozdiari, Osnat Penn, Sagiv Shifman, Santhosh Girirajan, Fereydoun Hormozdiari
Format: Article
Language:English
Published: BMC 2019-10-01
Series:Genome Medicine
Subjects:
Epilepsy
Autism
Intellectual disability
Developmental disability
Module discovery
De novo mutation
Online Access:http://link.springer.com/article/10.1186/s13073-019-0678-y

Internet

http://link.springer.com/article/10.1186/s13073-019-0678-y

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