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Thymidine to Cytosine Transition Abnormality
A point mutation involving the substitution of Cytosine (a pyrimidine base) for Thymidine (a pyrimidine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically. (NCI Thesaurus)
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Human Thymidine Kinases (Thymidine Kinase Family) catalyze thymidine phosphorylation via ATP to deoxythymidine monophosphate.
A chemical compound found in DNA. Also used as treatment for mucositis.
