Frequency of Werner helicase 1367 polymorphism and age-related morbidity in an elderly Brazilian population
Werner syndrome (WS) is a premature aging disease caused by a mutation in the WRN gene. The gene was identified in 1996 and its product acts as a DNA helicase and exonuclease. Some specific WRN polymorphic variants were associated with increased risk for cardiovascular diseases. The identification o...
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| Asıl Yazarlar: | , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Associação Brasileira de Divulgação Científica
2005-07-01
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| Seri Bilgileri: | Brazilian Journal of Medical and Biological Research |
| Konular: | |
| Online Erişim: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2005000700008 |
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