Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15)

American Journal of Ophthalmology

Volumn 136, Issue 5, 2003, Pages 933-935

  Martin, Tammy M ^a   Doyle, Trudy M ^a   Smith, Justine R ^a   Dinulescu, Denis ^a   Rust, Kristal ^a   Rosenbaum, James T ^a,b  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYRIBONUCLEOPROTEIN; DNA;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; EXON; FEMALE; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENE MUTATION; GENE NOD2; GENE SEQUENCE; HUMAN; MALE; MEDICAL RECORD; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SARCOIDOSIS; STATISTICAL SIGNIFICANCE; UVEITIS;

EID: 0142257968     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(03)00892-4     Document Type: Article

References (7)

1. Blau E.B. Familial granulomatous arthritis, iritis, and rash. J Pediatrics. 107:1985;689-693.
2. Jabs D.A., Houk J.L., Bias W.B., Arnett F.C. Familial granulomatous synovitis, uveitis, and cranial neuropathies. Am J Med. 78:1985;801-804.
3. Miceli-Richard C., Lesage S., Rybojad M., et al. CARD15 mutations in Blau syndrome. Nat Genet. 29:2001;19-20.
4. Ogura Y., Bonen D.K., Inohara N., et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature. 411:2001;603-606.
5. Hugot J.-P., Chamaillard M., Zouali H., et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature. 411:2001;599-603.
6. Lesage S., Zouali H., Cezard J.P., et al. CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. Am J Hum Genet. 70:2002;845-857.
7. Rybicki B.A., Maliarik M.J., Bock C.H., et al. The Blau syndrome gene is not a major risk factor for sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis. 16:1999;203-208.