Immunophenotyping in peripheral blood mononuclear cells, aqueous humour and vitreous in a blau syndrome patient caused by a novel nod2 mutation

International Journal of Immunogenetics

Volumn 38, Issue 3, 2011, Pages 233-242

  Jimenez Martinez, M C ^a,b   Cruz, F ^c   Groman Lupa, S ^b   Zenteno, J C ^a,b  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b INSTITUTE OF OPHTHALMOLOGY CONDE DE VALENCIANA   (Mexico)

^c INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE; DNA; INTERLEUKIN 6; INTERLEUKIN 8;

AQUEOUS HUMOR; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLAU SYNDROME; CASE REPORT; CHILD; FEMALE; FLOW CYTOMETRY; GENE MUTATION; HUMAN; HUMAN CELL; IMMUNOPATHOLOGY; IMMUNOPHENOTYPING; NUCLEOTIDE SEQUENCE; ONSET AGE; PERIPHERAL BLOOD MONONUCLEAR CELL; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SARCOIDOSIS; T LYMPHOCYTE; VITREOUS BODY;

AQUEOUS HUMOR; BASE SEQUENCE; CHILD, PRESCHOOL; CRANIAL NERVE DISEASES; CYTOKINES; FEMALE; HETEROZYGOTE; HUMANS; IMMUNOPHENOTYPING; LEUKOCYTES, MONONUCLEAR; MUTATION; NOD2 SIGNALING ADAPTOR PROTEIN; PHENOTYPE; RECEPTORS, CHEMOKINE; SYNOVITIS; TOLL-LIKE RECEPTORS; UVEITIS; VITREOUS BODY;

EID: 79956289017     PISSN: 17443121     EISSN: 1744313X     Source Type: Journal    
DOI: 10.1111/j.1744-313X.2011.00998.x     Document Type: Article

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