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Oxidative nucleotide damage and superoxide dismutase expression in the brains of xeroderma pigmentosum group A and Cockayne syndrome

✍ Scribed by Masaharu Hayashi; Satoshi Araki; Jun Kohyama; Kei Shioda; Ryo Fukatsu


Book ID
113498139
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
166 KB
Volume
27
Category
Article
ISSN
0387-7604

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The human diseases xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy are caused by mutations in a set of interacting gene products, which carry out the process of nucleotide excision repair. The majority of the genes have now been cloned and many mutations in the genes identified. Th