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xeroderma pigmentosum, group d
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External
Examination of Clinical and Laboratory Abnormalities in Patients With Defective DNA Repair: Xeroderma Pigmentosum, Cockayne Syndrome, or Trichothiodystrophy
PubMed Links
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ERCC2
Polymorphisms in the human XPD (ERCC2) gene, DNA repair capacity and cancer susceptibility: an appraisal
Transcription of eukaryotic protein-coding genes
Cancer Gene Census
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ERCC2
Somatic tumors
Tumor types germline
skin basal cell, skin squamous cell, melanoma
Cancer Syndrom
xeroderma pigmentosum (D)
Translocation partner
Name
excision repair cross-complementing rodent repair deficiency, complementation group 2 (xeroderma pigmentosum D)
Chromosome banding
19q13.2-q13.3
Cancer molecular gen.
Rec
Mutation type
Mis, N, F, S
Other syndrome disease
Definition
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