Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

BACKGROUND: Specific language impairment (SLI) is a common neurodevelopmental disorder, observed in 5–10 % of children. Family and twin studies suggest a strong genetic component, but relatively few candidate genes have been reported to date. A recent genome-wide association study (GWAS) described t...

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Vydáno v:J Neurodev Disord
Hlavní autoři: Pettigrew, Kerry A., Frinton, Emily, Nudel, Ron, Chan, May T. M., Thompson, Paul, Hayiou-Thomas, Marianna E., Talcott, Joel B., Stein, John, Monaco, Anthony P., Hulme, Charles, Snowling, Margaret J., Newbury, Dianne F., Paracchini, Silvia
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4908686/
https://ncbi.nlm.nih.gov/pubmed/27307794
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-016-9157-6
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