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Fanconi anemia and DNA repair
Abstract
Fanconi anemia (FA) is an autosomal recessive disorder caused by defects in at least eight distinct genes FANCA, B, C, D1, D2, E, F and G. The clinical phenotype of all FA complementation groups is similar and is characterized by progressive bone marrow failure, cancer proneness and typical birth defects. The principal cellular phenotype is hypersensitivity to DNA damage, particularly interstrand DNA crosslinks. The FA proteins constitute a...
Paper Details
Title
Fanconi anemia and DNA repair
Published Date
Oct 1, 2001
Journal
Volume
10
Issue
20
Pages
2253 - 2259
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