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268th ENMC workshop - Genetic diagnosis, clinical classification, outcome measures, and biomarkers in Facioscapulohumeral Muscular Dystrophy (FSHD): Relevance for clinical trials.

Montagnese, Federica; de Valle, Katy; Lemmers, Richard JLF; Mul, Karlien; Dumonceaux, Julie; Voermans, Nicol; (2023) 268th ENMC workshop - Genetic diagnosis, clinical classification, outcome measures, and biomarkers in Facioscapulohumeral Muscular Dystrophy (FSHD): Relevance for clinical trials. Neuromuscular Disorders , 33 (5) pp. 447-462. 10.1016/j.nmd.2023.04.005. Green open access

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Type: Article
Title: 268th ENMC workshop - Genetic diagnosis, clinical classification, outcome measures, and biomarkers in Facioscapulohumeral Muscular Dystrophy (FSHD): Relevance for clinical trials.
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.nmd.2023.04.005
Publisher version: https://doi.org/10.1016/j.nmd.2023.04.005
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: Clinical trials, Dystrophy, ENMC, Facioscapulohumeral
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Developmental Neurosciences Dept
URI: https://discovery-pp.ucl.ac.uk/id/eprint/10169166
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