Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.
<h4>Background</h4> <p>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 associ...
المؤلفون الرئيسيون: | Pettigrew, K, Frinton, E, Nudel, R, Chan, M, Thompson, P, Hayiou-Thomas, M, Talcott, J, Stein, J, Monaco, A, Hulme, C, Snowling, M, Newbury, D, Paracchini, S |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
BioMed Central
2016
|
مواد مشابهة
-
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
حسب: Newbury, D, وآخرون
منشور في: (2016) -
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures
حسب: Martinelli, A, وآخرون
منشور في: (2021) -
The DCDC2 deletion is not a risk factor for dyslexia
حسب: Scerri, T, وآخرون
منشور في: (2017) -
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
حسب: Scerri, T, وآخرون
منشور في: (2012) -
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
حسب: Nudel, R, وآخرون
منشور في: (2014)