Zobrazeno 1 - 1
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pro vyhledávání: '"Turaga Ramachander VN"'
Publikováno v:
BMC Genomics, Vol 11, Iss 1, p 127 (2010)
Abstract Background Werner Syndrome (WS) is a rare disorder characterized by the premature onset of a number of age-related diseases. The gene responsible for WS encodes a DNA helicase/exonuclease protein believed to affect different aspects of trans
Externí odkaz:
https://doaj.org/article/54eea969a68046628f9f3848058b0ef0
