Female-specific association of C-C chemokine receptor 5 gene polymorphisms with Löfgren's syndrome

Journal of Molecular Medicine

Volumn 86, Issue 5, 2008, Pages 553-561

  Fischer, Annegret ^a   Valentonyte, Ruta ^a   Nebel, Almut ^a   Nothnagel, Michael ^a   Müller Quernheim, Joachim ^b   Schürmann, Manfred ^c   Schreiber, Stefan ^a  

^a UNIVERSITY OF KIEL   (Germany)

^b UNIVERSITY OF FREIBURG   (Germany)

^c UNIVERSITY OF LÜBECK   (Germany)

Author keywords

CCR5; HHC haplotype; Sarcoidosis; Sex

Indexed keywords

CHEMOKINE RECEPTOR CCR5;

ACUTE DISEASE; ALLELE; ARTICLE; CHRONIC DISEASE; COMPARATIVE STUDY; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENETIC ASSOCIATION; GENETIC MARKER; GENOTYPE; HAPLOTYPE; HUMAN; LOFGREN SYNDROME; LUNG PARENCHYMA; LUNG SARCOIDOSIS; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PROMOTER REGION; RECEPTOR GENE; SARCOIDOSIS; SEX RATIO; SINGLE NUCLEOTIDE POLYMORPHISM;

ABNORMALITIES, MULTIPLE; CASE-CONTROL STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC MARKERS; GERMANY; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, CCR5; SARCOIDOSIS; SEX CHARACTERISTICS; SYNDROME;

EID: 43049092928     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00109-008-0315-5     Document Type: Article

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