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Journal article

Unravelling neurogenetic networks implicated in developmental language disorders.

Abstract:

Childhood syndromes disturbing language development are common and display high degrees of heritability. In most cases, the underlying genetic architecture is likely to be complex, involving multiple chromosomal loci and substantial heterogeneity, which makes it difficult to track down the crucial genomic risk factors. Investigation of rare Mendelian phenotypes offers a complementary route for unravelling key neurogenetic pathways. The value of this approach is illustrated by the discovery th...

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Publication status:
Published

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Publisher copy:
10.1042/bst0371263

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author
Journal:
Biochemical Society transactions
Volume:
37
Issue:
Pt 6
Pages:
1263-1269
Publication date:
2009-12-01
DOI:
EISSN:
1470-8752
ISSN:
0300-5127
Language:
English
Keywords:
Pubs id:
pubs:34971
UUID:
uuid:cb3ec609-8d93-4c34-bd7c-a44fb306a5b0
Local pid:
pubs:34971
Source identifiers:
34971
Deposit date:
2012-12-19

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