Heritable genetic alterations in a xeroderma pigmentosum group G/Cockayne syndrome pedigree

Mutation Research - DNA Repair

Volumn 385, Issue 2, 1997, Pages 107-114

  Okinaka, Richard T ^a   Perez Castro, Ana V ^a   Sena, Anthony ^b   Laubscher, Kevin ^a   Strniste, Gary F ^a   Park, Min S ^a   Hernandez, Rudy ^a   MacInnes, Mark A ^a   Kraemer, Kenneth H ^c  

^a LOS ALAMOS NATIONAL LABORATORY   (United States)

^b Northern New Mexico College   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Cockayne Syndrome; Xeroderma pigmentosum

Indexed keywords

ARTICLE; BLOOD CELL; CASE REPORT; CELL CULTURE; COCKAYNE SYNDROME; GENETIC MARKER; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; MUTATION; PRIORITY JOURNAL; SKIN CELL; XERODERMA PIGMENTOSUM;

CELLS, CULTURED; COCKAYNE SYNDROME; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; ENDONUCLEASES; EXONS; FEMALE; GENES; GENETIC MARKERS; HUMANS; MALE; NUCLEAR PROTEINS; PEDIGREE; POINT MUTATION; POLYMORPHISM, GENETIC; RNA SPLICING; RNA, MESSENGER; TRANSCRIPTION FACTORS; XERODERMA PIGMENTOSUM;

EID: 0031439763     PISSN: 09218777     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0921-8777(97)00031-1     Document Type: Article

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