Xeroderma pigmentosum: clues to understanding cancer initiation
Xeroderma pigmentosum (XP) type C is a rare autosomal recessive disorder that occurs because of inactivation of the xeroderma pigmentosum group C (XPC) protein, which is an important DNA damage recognition protein involved in DNA nucleotide excision repair (NER). This defect, which prevents removal...
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Main Authors: | , , , , , , , |
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Format: | Book |
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Wolters Kluwer Medknow Publications,
2010-09-01T00:00:00Z.
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Internet
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A1234.567 |
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Copy 1 | Available |