Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
An exploratory genome-wide copy number variant (CNV) study was performed in 127 independent cases with specific language impairment (SLI), their first-degree relatives (385 individuals) and 269 population controls. Language-impaired cases showed an increased CNV burden in terms of the average number...
Main Authors: | Simpson, N, Ceroni, F, Reader, R, Covill, L, Knight, J, Hennessy, E, Bolton, P, Conti-Ramsden, G, O'Hare, A, Baird, G, Fisher, S, Newbury, D |
---|---|
Format: | Journal article |
Language: | English |
Published: |
Nature Publishing Group
2015
|
Similar Items
-
Associations of HLA alleles with specific language impairment.
by: Nudel, R, et al.
Published: (2014) -
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
by: Nudel, R, et al.
Published: (2014) -
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
by: Nudel, R, et al.
Published: (2014) -
Genome-Wide Studies of Specific Language Impairment.
by: Reader, R, et al.
Published: (2014) -
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
by: Simpson, N, et al.
Published: (2014)