Evidence of an association between desmoglein 3 haplotypes and pemphigus vulgaris

British Journal of Dermatology

Volumn 154, Issue 1, 2006, Pages 67-71

  Capon, F ^a,e   Bharkhada, J ^a   Cochrane, N E ^a   Mortimer, N J ^b   Setterfield, J F ^c   Reynaert, S ^c   Black, M M ^c   Vaughan, R W ^d   Trembath, R C ^a   Harman, K E ^b  

^a UNIVERSITY OF LEICESTER   (United Kingdom)

^b UNIVERSITY HOSPITALS OF LEICESTER NHS TRUST   (United Kingdom)

^c ST THOMAS HOSPITAL   (United Kingdom)

^d GUY S HOSPITAL   (United Kingdom)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Autoimmune disease; Desmoglein 3; Genetic susceptibility; Pemphigus vulgaris

Indexed keywords

DESMOGLEIN 3;

ALLELE; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HAPLOTYPE; HEREDITY; HUMAN; INDIA; MAJOR CLINICAL STUDY; PEMPHIGUS VULGARIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED KINGDOM;

CASE-CONTROL STUDIES; DESMOGLEIN 3; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HLA-DR ANTIGENS; HUMANS; LINKAGE DISEQUILIBRIUM; PEMPHIGUS; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 33644922383     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2005.06882.x     Document Type: Article

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