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- W2040822029 abstract "Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenitalBallew et al. (2013)Journal of Human Genetics 132: 473–480.Constitutional mutations in RTEL1 cause severe dyskeratosis congenitaWalne et al. (2013)American Journal of Human Genetics 92 (3): 448–453." @default.
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- W2040822029 date "2013-05-27" @default.
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- W2040822029 title "Telomere shortening by mutations in theRTEL1helicase cause severe form of dyskeratosis congenita, Hoyerall-Hreidarsson syndrome" @default.
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- W2040822029 doi "https://doi.org/10.1111/cge.12175" @default.
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