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- W1971438029 abstract "Werner syndrome (WS) is one of a group of human genetic diseases that have recently been linked to deficits in cellular helicase function. We review the spectrum of WS-associated WRN mutations, the organization and potential functions of the WRN protein, and potential mechanistic links between the loss of WRN function and pathogenesis of the WS clinical and cellular phenotypes. Hum Mutat 13:271–279, 1999. © 1999 Wiley-Liss, Inc." @default.
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- W1971438029 date "1999-01-01" @default.
- W1971438029 modified "2023-10-11" @default.
- W1971438029 title "WRN mutations in Werner syndrome" @default.
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- W1971438029 doi "https://doi.org/10.1002/(sici)1098-1004(1999)13:4<271::aid-humu2>3.0.co;2-q" @default.
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