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Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family
Context: Dyslexia is a common disorder with a strong genetic component, but despite significant research effort, the aetiology is still largely unknown. Objective: To identify loci contributing to dyslexia risk. Methods: This was a genomewide linkage analysis in a single large family. Dutch families...
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| Main Authors: | , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BMJ Group
2004
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735895/ https://ncbi.nlm.nih.gov/pubmed/15342694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2003.012294 |
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