A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy

Human Mutation

Volumn 14, Issue 1, 1999, Pages 9-22

  Cleaver, James E ^a   Thompson, Larry H ^b   Richardson, Audrey S ^c   States, J Christopher ^c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b LAWRENCE LIVERMORE NATIONAL LABORATORY   (United States)

^c WAYNE STATE UNIVERSITY   (United States)

Author keywords

Cockayne syndrome; DNA repair; Mutation; Trichothiodystrophy; Xeroderma pigmentosum

Indexed keywords

DNA BINDING PROTEIN; GENE PRODUCT;

COCKAYNE SYNDROME; DIAGNOSTIC ACCURACY; DISEASE ASSOCIATION; DNA REPAIR; FRAMESHIFT MUTATION; GENE MUTATION; HUMAN; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; REVIEW; SKIN DISEASE; STRUCTURE ACTIVITY RELATION; TRICHOTHIODYSTROPHY; ULTRAVIOLET RADIATION; XERODERMA PIGMENTOSUM;

COCKAYNE SYNDROME; DNA REPAIR; HAIR DISEASES; HUMANS; MUTATION; PHOTOSENSITIVITY DISORDERS; ULTRAVIOLET RAYS; XERODERMA PIGMENTOSUM;

EID: 0032993689     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1999)14:1<9::AID-HUMU2>3.0.CO;2-6     Document Type: Review

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