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Genome‐wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis‐regulation of BORCS7, AS3MT, and NT5C2 in the human brain
Chromosome 10q24.32‐q24.33 is one of the most robustly supported risk loci to emerge from genome‐wide association studies (GWAS) of schizophrenia. However, extensive linkage disequilibrium makes it difficult to distinguish the actual susceptibility gene(s) at the locus, limiting its value for improv...
Wedi'i Gadw mewn:
Cyhoeddwyd yn: | Am J Med Genet B Neuropsychiatr Genet |
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Prif Awduron: | , , , , , |
Fformat: | Artigo |
Iaith: | Inglês |
Cyhoeddwyd: |
John Wiley and Sons Inc.
2016
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Pynciau: | |
Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4988385/ https://ncbi.nlm.nih.gov/pubmed/27004590 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32445 |
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