A prospective study of filaggrin null mutations in keratoconus patients with or without atopic disorders

Dermatology

Volumn 222, Issue 4, 2011, Pages 336-341

  Droitcourt, C ^a,c   Touboul, D ^a   Ged, C ^b   Ezzedine, K ^a,b   Cario Andre M ^b   De Verneuil, H ^b   Colin, J ^a   Taieb A ^a,b  

^a BORDEAUX UNIVERSITY HOSPITAL   (France)

^b UNIVERSITÉ DE BORDEAUX   (France)

^c HÔPITAL SAINT ANDRÉ   (France)

Author keywords

Atopic dermatitis; Filaggrin; Keratoconus

Indexed keywords

FILAGGRIN;

ADULT; ARTICLE; ATOPIC DERMATITIS; ATOPY; CLINICAL ASSESSMENT; CONTROLLED STUDY; CORNEA EPITHELIUM; DISEASE ASSOCIATION; FEMALE; GENE EXPRESSION; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; HUMAN; KERATOCONUS; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL; PROSPECTIVE STUDY;

ADOLESCENT; ADULT; CHILD; DERMATITIS, ATOPIC; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INTERMEDIATE FILAMENT PROTEINS; KERATOCONUS; MALE; MIDDLE AGED; MUTATION; PREVALENCE; PROSPECTIVE STUDIES; YOUNG ADULT;

EID: 80052449219     PISSN: 10188665     EISSN: 14219832     Source Type: Journal    
DOI: 10.1159/000328408     Document Type: Article

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