Filaggrin loss-of-function variant contributes to atopic dermatitis risk in the population of Northern Germany
- 23 August 2006
- journal article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 155 (5) , 1093-1094
- https://doi.org/10.1111/j.1365-2133.2006.07500.x
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitisNature Genetics, 2006
- PopGen: Population-Based Recruitment of Patients and Controls for the Analysis of Complex Genotype-Phenotype RelationshipsPublic Health Genomics, 2006
- Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgarisNature Genetics, 2006
- Lack of association of SPINK5 polymorphisms with nonsyndromic atopic dermatitis in the population of Northern GermanyBritish Journal of Dermatology, 2005
- Genetics of Crohn disease, an archetypal inflammatory barrier diseaseNature Reviews Genetics, 2005
- Sarcoidosis is associated with a truncating splice site mutation in BTNL2Nature Genetics, 2005
- Genetic variation in DLG5 is associated with inflammatory bowel diseaseNature Genetics, 2004
- Efficient Multipoint Linkage Analysis through Reduction of Inheritance SpaceAmerican Journal of Human Genetics, 2001
- Filaggrin: A Keratin Filament Associated ProteinaAnnals of the New York Academy of Sciences, 1985
- Diagnostic Features of Atopic DermatitisActa Dermato-Venereologica, 1980