📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome. (2017)

First Author: Sleven H

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