Disorders of nucleotide excision repair
Author:
Publisher
Elsevier
Reference43 articles.
1. Rare diseases provide rare insights into nucleotide excision repair, transcription-coupled repair, TFIIH, aging and cancer;Bohr;DNA Repair (Amst),2005
2. Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy;Boyle;Hum Mutat,2008
3. Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene;Broughton;Hum Mol Genet,2001
4. Clinical implications of the basic defects in Cockayne syndrome and xeroderma pigmentosum and the DNA lesions responsible for cancer, neurodegeneration and aging;Cleaver;Mech Ageing Dev,2008
5. Dwarfism with retinal atrophy and deafness;Cockayne;Arch Dis Child,1936
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