Contrasting association of a non-synonymous leptin receptor gene polymorphism with Wegener's granulomatosis and Churg-Strauss syndrome.

Rheumatology (Oxford, England)

Volumn 49, Issue 5, 2010, Pages 907-914

  Wieczorek, Stefan ^a   Holle, Julia U ^b   Bremer, Jan P ^b   Wibisono, David ^b   Moosig, Frank ^b   Fricke, Harald ^b   Assmann, Gunter ^b   Harper, Lorraine ^b   Arning, Larissa ^b   Gross, Wolfgang L ^b   Epplen, Joerg T ^b  

^a RUHR UNIVERSITY BOCHUM   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

GHRELIN; GHRELIN RECEPTOR; LEPTIN; LEPTIN RECEPTOR;

ARTICLE; CASE CONTROL STUDY; CAUCASIAN; CHURG STRAUSS SYNDROME; FEMALE; GENE FREQUENCY; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; HAPLOTYPE; HUMAN; MALE; MIDDLE AGED; WEGENER GRANULOMATOSIS;

CASE-CONTROL STUDIES; CHURG-STRAUSS SYNDROME; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GHRELIN; HAPLOTYPES; HUMANS; LEPTIN; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; RECEPTORS, GHRELIN; RECEPTORS, LEPTIN; WEGENER GRANULOMATOSIS;

EID: 79952462015     PISSN: None     EISSN: 14620332     Source Type: Journal    
DOI: 10.1093/rheumatology/kep420     Document Type: Article

References (0)