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Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner
BACKGROUND: Chromosome 17q21.31 contains a common inversion polymorphism of approximately 900 kb in populations with European ancestry. Two divergent MAPT haplotypes, H1 and H2 are described with distinct linkage disequilibrium patterns across the region reflecting the inversion status at this locus...
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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3582489/ https://ncbi.nlm.nih.gov/pubmed/22950410 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-458 |
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