Molecular Pathogenesis of Fanconi Anemia

Volume: 75, Issue: 2, Pages: 123 - 128
Published: Feb 1, 2002
Abstract
Fanconi anemia (FA) is a rare autosomal recessive chromosomal breakage disorder characterized by the childhood onset of aplastic anemia, developmental defects, cancer susceptibility, and cellular hypersensitivity to DNA—cross-linking agents. FA patients can be divided into at least 8 complementation groups (FA-A, FA-B, FA-C, FA-D1, FA-D2, FA-E, FA-F, and FA-G). FA proteins encoded by 6 cloned FA genes (FANCA,FANCC,FANCD2,FANCE,FANCF, andFANCG)...
Paper Details
Title
Molecular Pathogenesis of Fanconi Anemia
Published Date
Feb 1, 2002
Volume
75
Issue
2
Pages
123 - 128
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