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

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