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WRN polymorphisms affect expression levels of plasminogen activator inhibitor type 1 in cultured fibroblasts
BACKGROUND: Recessive mutations in WRN gene eliminate WRN protein function (helicase) and cause Werner syndrome. One of the most important clinical features of Werner syndrome patients are the premature onset and accelerated atherosclerosis process. Studies carried out on polymorphic WRN locus have...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292137/ https://www.ncbi.nlm.nih.gov/pubmed/18312663 http://dx.doi.org/10.1186/1471-2261-8-5 |