Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease

Journal of Human Genetics

Volumn 47, Issue 9, 2002, Pages 469-472

  Yamazaki, K ^a   Takazoe, M ^b   Tanaka, T ^b   Kazumori, T ^b   Nakamura, Y ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b Social Insurance Central General Hospital   (Japan)

Author keywords

Crohn's disease; IBD1; Japanese population; NOD2 CARD15; Single nucleotide polymorphism (SNP)

Indexed keywords

ARTICLE; CHROMOSOME 16; CONTROLLED STUDY; CROHN DISEASE; DNA DETERMINATION; DNA SEQUENCE; FRAMESHIFT MUTATION; GENE; GENE MUTATION; GENE NOD2; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; JAPAN; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; RISK FACTOR; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

CARRIER PROTEINS; CROHN DISEASE; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; GENOTYPE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; JAPAN; MUTATION; NOD2 SIGNALING ADAPTOR PROTEIN; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; VARIATION (GENETICS);

EID: 0036373539     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380200067     Document Type: Article

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