The human XPG gene: Gene architecture, alternative splicing and single nucleotide polymorphisms

Nucleic Acids Research

Volumn 29, Issue 7, 2001, Pages 1443-1452

  Emmert, Steffen ^a,c   Schneider, Thomas D ^b   Khan, Sikandar G ^a   Kraemer, Kenneth H ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

^b NATIONAL CANCER INSTITUTE   (United States)

^c UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; ENDONUCLEASE; POLYDEOXYRIBONUCLEOTIDE SYNTHASE;

ALTERNATIVE RNA SPLICING; ANALYSIS; ARTICLE; CANCER SUSCEPTIBILITY; COCKAYNE SYNDROME; CONTROLLED STUDY; DNA SEQUENCE; EXON; GENE DELETION; GENE FREQUENCY; GENE FUNCTION; GENE SEQUENCE; GENE STRUCTURE; GENETIC DISORDER; HUMAN; HUMAN CELL; INFORMATION; INTRON; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; XERODERMA PIGMENTOSUM;

EID: 0035312291     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/29.7.1443     Document Type: Article

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