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xeroderma pigmentosum, group b
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ERCC3
Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3
Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair
Three functional classes of transcriptional activation domain
Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein
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ERCC3
Somatic tumors
Tumor types germline
skin basal cell, skin squamous cell, melanoma
Cancer Syndrom
xeroderma pigmentosum (B)
Translocation partner
Name
excision repair cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing)
Chromosome banding
2q21
Cancer molecular gen.
Rec
Mutation type
Mis, S
Other syndrome disease
Definition
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Pathways
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