Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
A locus on chromosome 2p12-16 has been implicated in dyslexia susceptibility by two independent linkage studies, including our own study of 119 nuclear twin-based families, each with at least one reading-disabled child. Nonetheless, no variant of any gene has been reported to show association with d...
Autors principals: | Francks, C, Fisher, S, Olson, R, Pennington, B, Smith, S, DeFries, J, Monaco, A |
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Format: | Journal article |
Idioma: | English |
Publicat: |
2002
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