TY  - JOUR
AU  - Carmona, F David
AU  - Martín, José-Ezequiel
AU  - Beretta, Lorenzo
AU  - Simeón, Carmen P
AU  - Carreira, Patricia E
AU  - Callejas, José Luis
AU  - Fernández-Castro, Mónica
AU  - Sáez-Comet, Luis
AU  - Beltrán, Emma
AU  - Camps, María Teresa
AU  - Egurbide, María Victoria
AU  - Airó, Paolo
AU  - Scorza, Raffaella
AU  - Lunardi, Claudio
AU  - Hunzelmann, Nicolas
AU  - Riemekasten, Gabriela
AU  - Witte, Torsten
AU  - Kreuter, Alexander
AU  - Distler, Jörg H W
AU  - Madhok, Rajan
AU  - Shiels, Paul
AU  - van Laar, Jacob M
AU  - Fonseca, Carmen
AU  - Denton, Christopher
AU  - Herrick, Ariane
AU  - Worthington, Jane
AU  - Schuerwegh, Annemie J
AU  - Vonk, Madelon C
AU  - Voskuyl, Alexandre E
AU  - Radstake, Timothy R D J
AU  - Martín, Javier
PY  - 2013
DO  - 10.1371/journal.pone.0054419
UR  - http://hdl.handle.net/10668/1942
T2  - PloS one
AB  - Systemic sclerosis (SSc) is a fibrotic autoimmune disease in which the genetic component plays an important role. One of the strongest SSc association signals outside the human leukocyte antigen (HLA) region corresponds to interferon (IFN) regulatory...
LA  - en
PB  - Public Library of Science
KW  - Factores reguladores del interferón
KW  - Predisposición genética a la enfermedad
KW  - Haplotipos
KW  - Polimorfismo de nucleótido simple
KW  - Lupus eritematoso sistémico
KW  - Desequilibrio de ligamiento
KW  - Grupo de ascendencia continental europea
KW  - Factores de riesgo
KW  - Medical Subject Headings::Named Groups::Persons::Population Groups::Continental Population Groups::European Continental Ancestry Group
KW  - Medical Subject Headings::Check Tags::Female
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Gene Frequency
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genetic Loci
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes
KW  - Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans
KW  - Medical Subject Headings::Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intracellular Signaling Peptides and Proteins::Adaptor Proteins, Signal Transducing::Interferon Regulatory Factors
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Linkage::Linkage Disequilibrium
KW  - Medical Subject Headings::Diseases::Immune System Diseases::Autoimmune Diseases::Lupus Erythematosus, Systemic
KW  - Medical Subject Headings::Check Tags::Male
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Phenotype
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic
KW  - Medical Subject Headings::Health Care::Environment and Public Health::Public Health::Epidemiologic Factors::Causality::Risk Factors
KW  - Medical Subject Headings::Diseases::Skin and Connective Tissue Diseases::Skin Diseases::Scleroderma, Systemic
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles
TI  - The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis
TY  - research article
ER  -