| 摘要 |
<p>The invention relates to the field of vasculopathy and the diagnosis and treatment thereof. The invention provides a method for screening for a disease locus associated with vasculopathy in humans comprising testing genomic DNA via linkage analysis for the presence of a polymorphism or an allelic variation within a microsatellite region on chromosome 3p21.1-p21.3 and an isolated and/or recombinant nucleic acid, or fragment thereof, corresponding to or derived from a disease locus associated with vasculopathy which in humans is located on chromosome 3p21.1-p21.3.</p> |
