The genetic basis of xeroderma pigmentosum and trichothiodystrophy syndromes

Cancer Surveys

Volumn 26, Issue , 1996, Pages 155-171

  Stary, Anne ^a  

^a Institute de Recherche sur le Cancer   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DNA REPAIR; GENE MUTATION; HUMAN; PRIORITY JOURNAL; RADIATION HAZARD; REVIEW; TRICHOTHIODYSTROPHY; ULTRAVIOLET RADIATION; XERODERMA PIGMENTOSUM;

DNA REPAIR; GENETIC PREDISPOSITION TO DISEASE; HAIR DISEASES; HUMANS; RADIATION TOLERANCE; SKIN NEOPLASMS; SYNDROME; ULTRAVIOLET RAYS; XERODERMA PIGMENTOSUM;

EID: 0029548435     PISSN: 02612429     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (3)

1. Bootsma D, Weeda G, Vermeulen W et al (1995) Nucleotide excision repair syndromes: molecular basis and clinical symptoms. Philosophical Transactions of the Royal Society of London B 347 75-81
2. Bredberg A, Kraemer KH and Seidman MM (1986) Restricted ultraviolet mutational spectrum in a shuttle vector propagated in xeroderma pigmentosum cells. Proceedings of the National Academy of Sciences of the USA 83 8273-8277
3. Broughton BC, Steingrimsdottir H, Weber CA and Lehmann AR (1994) Mutations in xeroderma pigmentosum group D DNA repair gene in patients with trichothiodystrophy. Nature Genetics 7 189-194