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Genetic toxicity base substitutions

The feature of all inherited disorders is a genetic defect, often the result of a single base substitution or deletion in the DNA. which results in the reduced synthesis of a particular protein or in the synthesis of a protein with an altered amino acid coniposiiion. A classical inborn error of metaholisni involves a missing or defective en/yme which causes a block on a metabolic pathway and the production of toxic metabolites. More than four thousand disorders involving single genes have been identified. [Pg.62]


See other pages where Genetic toxicity base substitutions is mentioned: [Pg.64]    [Pg.10]    [Pg.39]    [Pg.87]    [Pg.31]    [Pg.174]    [Pg.339]    [Pg.339]    [Pg.168]    [Pg.485]   
See also in sourсe #XX -- [ Pg.264 , Pg.265 ]




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