Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene

Proceedings of the National Academy of Sciences of the United States of America

Volumn 94, Issue 16, 1997, Pages 8658-8663

  Taylor, Elaine M ^a   Broughton, Bernard C ^a   Botta, Elena ^b   Stefanini, Miria ^b   Sarasin, Alain ^c   Jaspers, Nicolaas G J ^d   Fawcett, Heather ^a   Harcourt, Susan A ^a   Arlett, Colin F ^a   Lehmann, Alan R ^a  

^a UNIVERSITY OF SUSSEX   (United Kingdom)

^b Ist Genet Biochim ed E   (Italy)

^c IFC1   (France)

^d ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

Nucleotide excision repair; Transcription factor TFIIH; UV irradiation

Indexed keywords

AMINO ACID; DNA; NUCLEOTIDE; PROTEIN; TRANSCRIPTION FACTOR;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; DNA DAMAGE; GENE; GENE MUTATION; HUMAN; HUMAN CELL; NONHUMAN; OPEN READING FRAME; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCHIZOSACCHAROMYCES POMBE; TRICHOTHIODYSTROPHY; XERODERMA PIGMENTOSUM;

CELL LINE; DNA HELICASES; DNA REPAIR; DNA-BINDING PROTEINS; FIBROBLASTS; HAIR DISEASES; HUMANS; MUTATION; PROTEINS; TRANSCRIPTION FACTORS; ULTRAVIOLET RAYS; XERODERMA PIGMENTOSUM; XERODERMA PIGMENTOSUM GROUP D PROTEIN;

SCHIZOSACCHAROMYCES POMBE;

EID: 12644310290     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.16.8658     Document Type: Article

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