Association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis-related calcinosis.

Duffus, Kate; López-Isac, Elena; Teruel, Maria; Simeón, Carmen Pilar; Carreria, Patricia; Ortego-Centeno, Norberto; Vicente, Esther; Worthington, Jane; Herrick, Ariane L; Martin, Javier

Duffus, Kate; López-Isac, Elena; Teruel, Maria; Simeón, Carmen Pilar; Carreria, Patricia; Ortego-Centeno, Norberto; Vicente, Esther; Worthington, Jane; Herrick, Ariane L; Martin, Javier.

Afiliación

Duffus K; Arthritis Research UK Centre for Genetics and Genomics, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
López-Isac E; Institute of Parasitology and Biomedicine López-Neyra, IPBLN-CSIC, PTS Granada, Granada, Spain.
Teruel M; Center for Genomics and Oncological Research Pfizer/University of Granada/Andalusian Government, GENYO, PTS Granada, Granada, Spain.
Simeón CP; Department of Internal Medicine, Valle de Hebrón Hospital, Barcelona, Spain.
Carreria P; Department of Rheumatology, 12 de Octubre University Hospital, Madrid, Spain.
Ortego-Centeno N; Department of Internal Medicine, Clinic University Hospital, Granada, Spain.
Vicente E; Department of Rheumatology, La Princesa Hospital, Madrid, Spain.
Worthington J; Arthritis Research UK Centre for Genetics and Genomics, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Herrick AL; Centre for Musculoskeletal Research, Salford Royal NHS Foundation Trust, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Martin J; NIHR Manchester Musculoskeletal Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.

Rheumatology (Oxford) ; 58(7): 1299-1301, 2019 07 01.

Article en En | MEDLINE | ID: mdl-30789234

Asunto(s)

Calcinosis/genética; Ligando OX40/genética; Polimorfismo de Nucleótido Simple; Esclerodermia Sistémica/genética; Estudios de Casos y Controles; Predisposición Genética a la Enfermedad; Humanos

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esclerodermia Sistémica / Calcinosis / Polimorfismo de Nucleótido Simple / Ligando OX40 Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

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