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  1. Article

    Open Access

    17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes

    Parkinson’s disease (PD) is genetically associated with the H1 haplotype of the MAPT 17q.21.31 locus, although the causal gene and variants underlying this association have not been identified.

    Kathryn R. Bowles, Derian A. Pugh, Yiyuan Liu, Tulsi Patel in Molecular Neurodegeneration (2022)

  2. No Access

    Article

    Regional localization and characterization of a DNA segment on the long arm of chromosome 21

    A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ hybridization. This segment is therefore situated on the boundary of the “pathological region” of Down syndr...

    D. N. Cooper, S. C. Niemann, J. R. Gosden, A. R. Mitchell, A. M. Goate in Human Genetics (1987)