Xeroderma pigmentosum group C in a French Caucasian patient with multiple melanoma and unusual long-term survival
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2008.08791.x/fullpdf
Reference23 articles.
1. Defective repair replication of DNA in xeroderma pigmentosum;Cleaver;Nature,1968
2. Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases;Kraemer;Arch Dermatol,1987
3. Melanoma and other skin cancers in xeroderma pigmentosum patients and mutation in their cells;Takebe;J Invest Dermatol,1989
4. Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair;Sugasawa;Mol Cell,1998
5. The genetics of the hereditary xeroderma pigmentosum syndrome;Stary;Biochimie,2002
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2. Structural modeling and analyses of genetic variations in the human XPC nucleotide excision repair protein;Journal of Biomolecular Structure and Dynamics;2023-03-08
3. Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis;Journal of Dermatological Science;2018-02
4. Atypical Clinical Presentation of Xeroderma Pigmentosum in a Patient Harboring a Novel Missense Mutation in the XPC Gene: The Importance of Clinical Suspicion;Dermatology;2015-08-05
5. Repair of UV photolesions in xeroderma pigmentosum group C cells induced by translational readthrough of premature termination codons;Proceedings of the National Academy of Sciences;2013-11-11
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