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• W2000507376 abstract "Dyskeratosis congenita (DC) is a rare syndrome, characterized by cutaneous abnormalities and premature death caused by bone marrow failure. In this issue of Genes & Development, Hockemeyer and colleagues (pp. 1773-1785) report a new mouse model that reconstitutes key features of DC. Disease phenotypes are generated by a POT1b deletion in a telomerase-deficient background that accelerates the shortening of telomeres by degradation." @default.
• W2000507376 created "2016-06-24" @default.
• W2000507376 creator A5020478244 @default.
• W2000507376 date "2008-07-01" @default.
• W2000507376 modified "2023-09-27" @default.
• W2000507376 title "POT of gold: modeling dyskeratosis congenita in the mouse" @default.
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• W2000507376 doi "https://doi.org/10.1101/gad.1695808" @default.
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