Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis

Journal of Investigative Dermatology

Volumn 126, Issue 8, 2006, Pages 1770-1775

  Sandilands, Aileen ^a   O'Regan, Gráinne M ^b   Liao, Haihui ^a   Zhao, Yiwei ^a   Terron Kwiatkowski, Ana ^a   Watson, Rosemarie M ^b   Cassidy, Andrew J ^a   Goudie, David R ^c   Smith, Frances J D ^a   McLean, W H Irwin ^a   Irvine, Alan D ^b  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

^b OUR LADY S CHILDREN S HOSPITAL   (Ireland)

^c NHS TAYSIDE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FILAGGRIN;

ARTICLE; ATOPIC DERMATITIS; CONTROLLED STUDY; FAMILY; FEMALE; GENE DELETION; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENETIC IDENTIFICATION; GENETIC PREDISPOSITION; HETEROZYGOTE; HOMOZYGOTE; HUMAN; ICHTHYOSIS VULGARIS; KERATOSIS PALMOPLANTARIS; MALE; MUTATIONAL ANALYSIS; PATHOGENESIS; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; RNA TRANSLATION; TANDEM REPEAT;

DERMATITIS, ATOPIC; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; ICHTHYOSIS VULGARIS; INTERMEDIATE FILAMENT PROTEINS; IRELAND; LINKAGE (GENETICS); MALE; PEDIGREE; PHENOTYPE; POINT MUTATION; PREVALENCE;

EID: 33746129175     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/sj.jid.5700459     Document Type: Article

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