TY  - GEN
AU  - Betz,Regina C
AU  - Pforr,Jana
AU  - Flaquer,Antonia
AU  - Redler,Silke
AU  - Hanneken,Sandra
AU  - Eigelshoven,Sibylle
AU  - Kortüm,Anne-Katrin
AU  - Tüting,Thomas
AU  - Lambert,Julien
AU  - De Weert,Jozef
AU  - Hillmer,Axel M
AU  - Schmael,Christine
AU  - Wienker,Thomas F
AU  - Kruse,Roland
AU  - Lutz,Gerhard
AU  - Blaumeiser,Bettina
AU  - Nöthen,Markus M
TI  - Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease
SN  - 1523-1747
PY  - 2007///1029
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Alopecia Areata
KW  - genetics
KW  - Case-Control Studies
KW  - Child
KW  - Child, Preschool
KW  - Comorbidity
KW  - Dermatitis, Atopic
KW  - Disease Progression
KW  - Female
KW  - Filaggrin Proteins
KW  - Humans
KW  - Intermediate Filament Proteins
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Risk Factors
KW  - Severity of Illness Index
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/sj.jid.5700915
ER  -