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Letter
Nature Genetics 37, 958–963 (1 September 2005) | doi:10.1038/ng1626
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
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Abstract
Fanconi anemia is a genetic disease characterized by genomic instability and cancer predisposition. Nine genes involved in Fanconi anemia have been identified; their products participate in a DNA damage–response network involving BRCA1 and BRCA2 (refs.
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