De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome. (2017)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2016.11.020
PubMed Identifier: 28017370
Publication URI: http://europepmc.org/abstract/MED/28017370
Type: Journal Article/Review
Volume: 100
Parent Publication: American journal of human genetics
Issue: 1
ISSN: 0002-9297