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...

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Detalles Bibliográficos
Autores principales: Simpson, Nuala H, Ceroni, Fabiola, Reader, Rose H, Covill, Laura E, Knight, Julian C, Hennessy, Elizabeth R, Bolton, Patrick F, Conti-Ramsden, Gina, O'Hare, Anne, Baird, Gillian, Fisher, Simon E, Newbury, Dianne F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592089/
https://www.ncbi.nlm.nih.gov/pubmed/25585696
http://dx.doi.org/10.1038/ejhg.2014.296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592089/
https://www.ncbi.nlm.nih.gov/pubmed/25585696
http://dx.doi.org/10.1038/ejhg.2014.296

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