From Wikipedia, the free encyclopedia
Dyslexia susceptibility 1, also known as DYX1, is a human gene.[1]
[edit] References
[edit] Further reading
- Brkanac Z, Chapman NH, Matsushita MM, et al. (2007). "Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.". Am. J. Med. Genet. B Neuropsychiatr. Genet. 144 (4): 556–60. doi:10.1002/ajmg.b.30471. PMID 17450541.
- Scerri TS, Fisher SE, Francks C, et al. (2005). "Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.". J. Med. Genet. 41 (11): 853–7. doi:10.1136/jmg.2004.018341. PMID 15520411.
- Cope NA, Hill G, van den Bree M, et al. (2005). "No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia.". Mol. Psychiatry 10 (3): 237–8. doi:10.1038/sj.mp.4001596. PMID 15477871.
- Wigg KG, Couto JM, Feng Y, et al. (2005). "Support for EKN1 as the susceptibility locus for dyslexia on 15q21.". Mol. Psychiatry 9 (12): 1111–21. doi:10.1038/sj.mp.4001543. PMID 15249932.
- Morris DW, Robinson L, Turic D, et al. (2000). "Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q.". Hum. Mol. Genet. 9 (5): 843–8. PMID 10749993.
- Nöthen MM, Schulte-Körne G, Grimm T, et al. (2000). "Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.". European child & adolescent psychiatry 8 Suppl 3: 56–9. PMID 10638372.
- Schulte-Körne G, Grimm T, Nöthen MM, et al. (1998). "Evidence for linkage of spelling disability to chromosome 15.". Am. J. Hum. Genet. 63 (1): 279–82. PMID 9634517.
- Grigorenko EL, Wood FB, Meyer MS, et al. (1997). "Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.". Am. J. Hum. Genet. 60 (1): 27–39. PMID 8981944.
- Bisgaard ML, Eiberg H, Møller N, et al. (1987). "Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.". Clin. Genet. 32 (2): 118–9. PMID 3652490.
