STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics

STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics

Abstract Background De novo loss of function mutations in STXBP1 are a relatively common cause of epilepsy and intellectual disability (ID). However, little is known about the types and severities of behavioural features associated with this genetic diagnosis. Methods To address this, we collected s...

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Bibliographic Details
Main Authors: Sinéad O’Brien, Elise Ng-Cordell, The DDD Study, Duncan E. Astle, Gaia Scerif, Kate Baker
Format: Article
Language:English
Published: BMC 2019-08-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
STXBP1
Epilepsy
Intellectual disability
Language
Social
Online Access:http://link.springer.com/article/10.1186/s11689-019-9278-9

Internet

http://link.springer.com/article/10.1186/s11689-019-9278-9

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