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: | , , , , , , , , , , , , |
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| التنسيق: | Journal article |
| اللغة: | English |
| منشور في: |
BioMed Central
2016
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