Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
A significant proportion of children have unexplained problems acquiring proficient linguistic skills despite adequate intelligence and opportunity. Developmental language disorders are highly heritable with substantial societal impact. Molecular studies have begun to identify candidate loci, but mu...
Main Authors: | Chen, XS, Reader, RH, Hoischen, A, Veltman, JA, Simpson, NH, Francks, C, Newbury, DF, Fisher, SE |
---|---|
Format: | Journal article |
Language: | English |
Published: |
Nature Research
2017
|
Similar Items
-
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
by: Simpson, N, et al.
Published: (2015) -
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
by: Pía Villanueva, et al.
Published: (2015-03-01) -
Genome-wide screening for DNA variants associated with reading and language traits.
by: Gialluisi, A, et al.
Published: (2014) -
Stage 2 registered report: variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis
by: Newbury, DF, et al.
Published: (2018) -
A genome wide screen for loci involved in specific language impairment
by: Newbury, D, et al.
Published: (2002)