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Werner综合征(Werner’ssyndrome,WS)是一种罕见的常染色体遗传的退行性疾病。人们对这种罕见的疾病给予了极大的关注,因为WS患者表现的症状是在进入成年后加速老化,WS发病机制的研究有可能对阐明衰老的机制和肿瘤发生的机制有借鉴作用。WS基因于1996年被确定,其后有关此病的研
Werner’s syndrome (WS) is a rare, autosomal genetic degenerative disease. Much attention has been paid to this rare disease because the symptoms of WS patients are accelerated aging after they enter adulthood. The study on the pathogenesis of WS may be useful for elucidating the mechanism of aging and the mechanism of tumorigenesis. WS gene was identified in 1996, followed by research on the disease