📣 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.

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. (2015)

First Author: Villanueva P

Attributed to: Investigation of the genetic causes of Specific Language Impairment (SLI) in an isolated Chilean population funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1371/journal.pgen.1004925

PubMed Identifier: 25781923

Publication URI: http://europepmc.org/abstract/MED/25781923

Type: Journal Article/Review

Volume: 11

Parent Publication: PLoS genetics

Issue: 3

ISSN: 1553-7390