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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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Detalhes bibliográficos
Main Authors: de Jong, Simone, Chepelev, Iouri, Janson, Esther, Strengman, Eric, van den Berg, Leonard H, Veldink, Jan H, Ophoff, Roel A
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2012
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Acesso em linha: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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