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Regulatory genomic regions active in immune cell types explain a large proportion of the genetic risk of multiple sclerosis.
Elangovan, Ramyiadarsini I; Disanto, Giulio; Berlanga-Taylor, Antonio J; Ramagopalan, Sreeram V; Handunnetthi, Lahiru.
Afiliación
  • Elangovan RI; Functional Genomics Unit, Department of Physiology, Anatomy and Genetics and Medical Research Council, University of Oxford, Oxford, UK.
  • Disanto G; 1] Functional Genomics Unit, Department of Physiology, Anatomy and Genetics and Medical Research Council, University of Oxford, Oxford, UK [2] Queen Mary University of London, Blizard Institute, Barts and The London School of Medicine and Dentistry, London, UK.
  • Berlanga-Taylor AJ; Functional Genomics Unit, Department of Physiology, Anatomy and Genetics and Medical Research Council, University of Oxford, Oxford, UK.
  • Ramagopalan SV; 1] Functional Genomics Unit, Department of Physiology, Anatomy and Genetics and Medical Research Council, University of Oxford, Oxford, UK [2] Queen Mary University of London, Blizard Institute, Barts and The London School of Medicine and Dentistry, London, UK.
  • Handunnetthi L; Functional Genomics Unit, Department of Physiology, Anatomy and Genetics and Medical Research Council, University of Oxford, Oxford, UK.
J Hum Genet ; 59(4): 211-5, 2014 Apr.
Article en En | MEDLINE | ID: mdl-24522295

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Secuencias Reguladoras de Ácidos Nucleicos / Esclerosis Múltiple Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Secuencias Reguladoras de Ácidos Nucleicos / Esclerosis Múltiple Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido