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Journal article

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

Abstract:

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 the first statistically significant association specifically for a SLI cohort between a missense variant (rs4280164) in the NOP9 gene and language-related phenotypes under a parent-of-or...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s11689-016-9157-6

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
Experimental Psychology
Role:
Author
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Funding agency for:
Newbury, D
Grant:
Career Development Fellowship
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Funding agency for:
Snowling, M
Grant:
WT082032MA
Royal Society More from this funder
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Publisher:
BioMed Central Publisher's website
Journal:
Journal of Neurodevelopmental Disorders Journal website
Volume:
8
Issue:
1
Pages:
24
Publication date:
2016-06-01
Acceptance date:
2016-06-03
DOI:
ISSN:
1866-1947 and 1866-1955
Pmid:
27307794
Source identifiers:
626325
Language:
English
Keywords:
Pubs id:
pubs:626325
UUID:
uuid:67635f0e-471a-4cbc-ad8b-5b718073a66c
Local pid:
pubs:626325
Deposit date:
2017-01-25

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