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Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study.
Chia, Ruth; Saez-Atienzar, Sara; Murphy, Natalie; Chiò, Adriano; Blauwendraat, Cornelis; Roda, Ricardo H; Tienari, Pentti J; Kaminski, Henry J; Ricciardi, Roberta; Guida, Melania; De Rosa, Anna; Petrucci, Loredana; Evoli, Amelia; Provenzano, Carlo; Drachman, Daniel B; Traynor, Bryan J.
Afiliación
  • Chia R; Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892; ruth.chia@nih.gov.
  • Saez-Atienzar S; Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892.
  • Murphy N; Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892.
  • Chiò A; Rita Levi Montalcini Department of Neuroscience, University of Turin, Turin 10126, Italy.
  • Blauwendraat C; Institute of Cognitive Sciences and Technologies, Consiglio Nazionale delle Ricerche, Rome 00185, Italy.
  • Roda RH; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892.
  • Kaminski HJ; Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD 21287.
  • Ricciardi R; Department of Neurology, Neurocenter, Helsinki University Hospital, Helsinki FIN-02900, Finland.
  • Guida M; Research Program of Translational Immunology, Faculty of Medicine, University of Helsinki, Helsinki FIN-02900, Finland.
  • De Rosa A; Department of Neurology and Rehabilitation Medicine, George Washington University, Washington, DC 20037.
  • Petrucci L; Department of Clinical and Experimental Medicine, University of Pisa, Pisa 56126, Italy.
  • Evoli A; Department of Clinical and Experimental Medicine, University of Pisa, Pisa 56126, Italy.
  • Provenzano C; Department of Clinical and Experimental Medicine, University of Pisa, Pisa 56126, Italy.
  • Drachman DB; Department of Clinical and Experimental Medicine, University of Pisa, Pisa 56126, Italy.
  • Traynor BJ; Institute of Neurology, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario "A. Gemelli" Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome 00168, Italy.
Proc Natl Acad Sci U S A ; 119(5)2022 02 01.
Article en En | MEDLINE | ID: mdl-35074870
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Transducción de Señal / Predisposición Genética a la Enfermedad / Miastenia Gravis Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Transducción de Señal / Predisposición Genética a la Enfermedad / Miastenia Gravis Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos