Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders. (2019)

First Author: Eaton CB
Attributed to:  MRC Centre for Neuropsychiatric Genetics and Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/epi.14722

PubMed Identifier: 30977115

Publication URI: http://europepmc.org/abstract/MED/30977115

Type: Journal Article/Review

Volume: 60

Parent Publication: Epilepsia

Issue: 5

ISSN: 0013-9580