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...

وصف كامل

التفاصيل البيبلوغرافية

المؤلفون الرئيسيون:	M.A.C. Smith, M.D.A. Silva, L.Q. Araujo, L.R. Ramos, R.W. Labio, R.R. Burbano, C.A. Peres, S.B. Andreoli, S.L.M. Payão, M.S. Cendoroglo
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	Associação Brasileira de Divulgação Científica 2005-07-01
سلاسل:	Brazilian Journal of Medical and Biological Research
الموضوعات:	WRN: codon 1367 polymorphism Age-related morbidities Elderly cohort study
الوصول للمادة أونلاين:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2005000700008
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!