Loss-of-function mutations in the Filaggrin gene and allergic contact sensitization to nickel

Journal of Investigative Dermatology

Volumn 128, Issue 6, 2008, Pages 1430-1435

  Novak, Natalija ^a,b   Baurecht, Hansjörg ^c   Schäfer, Torsten ^d   Rodriguez, Elke ^e   Wagenpfeil, Stefan ^c   Klopp, Norman ^b   Heinrich, Joachim ^b   Behrendt, Heidrun ^e   Ring, Johannes ^e   Wichmann, Erich ^b   Illig, Thomas ^b   Weidinger, Stephan ^e  

^a UNIVERSITY OF BONN   (Germany)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^d UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^e TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CONTACT ALLERGEN; NICKEL;

ADULT; ARTICLE; ATOPIC DERMATITIS; DRY SKIN; FEMALE; FILAGGRIN GENE; GENE; GENE FUNCTION; GENE MUTATION; HEREDITY; HUMAN; ICHTHYOSIS VULGARIS; KERATOSIS; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; RISK FACTOR; SKIN ALLERGY;

EID: 43749107303     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/sj.jid.5701190     Document Type: Article

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