Cargando…
An investigation of NFXL1, a gene implicated in a study of specific language impairment
BACKGROUND: A recent study identified NFXL1 as a candidate gene for specific language impairment. The protein encoded by this gene is predicted to be a transcription factor based on domain similarities with NFX1, a repressor of HLA class II genes, which have themselves been implicated in specific la...
Autor principal: | Nudel, Ron |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822306/ https://www.ncbi.nlm.nih.gov/pubmed/27053962 http://dx.doi.org/10.1186/s11689-016-9146-9 |
Ejemplares similares
-
Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment
por: Villanueva, Pía, et al.
Publicado: (2015) -
Correction: Exome Sequencing in an Admixed Isolated Population IndicatesNFXL1 Variants Confer a Risk for Specific Language Impairment
por: Villanueva, Pía, et al.
Publicado: (2015) -
Genome-Wide Studies of Specific Language Impairment
por: Reader, Rose H., et al.
Publicado: (2014) -
Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants
por: Nudel, Ron, et al.
Publicado: (2021) -
Correction: Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants
por: Nudel, Ron, et al.
Publicado: (2023)