Evaluation of blood gene expression levels in facioscapulohumeral muscular dystrophy patients.

Signorelli, M; Mason, A G; Mul, K; Evangelista, T; Mei, H; Voermans, N; Tapscott, S J; Tsonaka, R; van Engelen, B G M; van der Maarel, S M; Spitali, P

Signorelli, M; Mason, A G; Mul, K; Evangelista, T; Mei, H; Voermans, N; Tapscott, S J; Tsonaka, R; van Engelen, B G M; van der Maarel, S M; Spitali, P.

Affiliation

Signorelli M; Department of Biomedical Data Sciences, Leiden University Medical Center, 2333 ZC, Leiden, The Netherlands. m.signorelli@lumc.nl.
Mason AG; Department of Human Genetics, Leiden University Medical Center, 2333 ZC, Leiden, The Netherlands.
Mul K; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Evangelista T; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Centre for Life, Newcastle, NE1 3BZ, UK.
Mei H; Sorbonne Université, AP-HP, INSERM, Centre de référence Des Maladies Neuromusculaires Nord/Est/Ile de France, Groupe Hospitalier Universitaire La Pitié-Salpêtrière, Paris, France.
Voermans N; Department of Biomedical Data Sciences, Leiden University Medical Center, 2333 ZC, Leiden, The Netherlands.
Tapscott SJ; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Tsonaka R; Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, 98109, USA.
van Engelen BGM; Department of Neurology, University of Washington, Seattle, WA, 98105, USA.
van der Maarel SM; Department of Biomedical Data Sciences, Leiden University Medical Center, 2333 ZC, Leiden, The Netherlands.
Spitali P; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

Sci Rep ; 10(1): 17547, 2020 10 16.

Article de En | MEDLINE | ID: mdl-33067535

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Muscles squelettiques / Protéines à homéodomaine / Dystrophie musculaire facio-scapulo-humérale / Protéines adaptatrices de la transduction du signal / Facteur de transcription PAX7 Type d'étude: Clinical_trials / Prognostic_studies Limites: Adult / Aged / Female / Humans / Male / Middle aged Langue: En Journal: Sci Rep Année: 2020 Type de document: Article Pays d'affiliation: Pays-Bas Pays de publication: Royaume-Uni

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