TY  - GEN
AU  - Marenholz,Ingo
AU  - Nickel,Renate
AU  - Rüschendorf,Franz
AU  - Schulz,Florian
AU  - Esparza-Gordillo,Jorge
AU  - Kerscher,Tamara
AU  - Grüber,Christoph
AU  - Lau,Susanne
AU  - Worm,Margitta
AU  - Keil,Thomas
AU  - Kurek,Michael
AU  - Zaluga,Elisabetha
AU  - Wahn,Ulrich
AU  - Lee,Young-Ae
TI  - Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march
SN  - 0091-6749
PY  - 2006///1204
KW  - Asthma
KW  - complications
KW  - Child
KW  - Eczema
KW  - Family
KW  - Female
KW  - Filaggrin Proteins
KW  - Genetic Predisposition to Disease
KW  - Heterozygote
KW  - Humans
KW  - Hypersensitivity, Immediate
KW  - Intermediate Filament Proteins
KW  - genetics
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
KW  - Polymerase Chain Reaction
KW  - Risk Factors
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.jaci.2006.07.026
ER  -