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Dystrophin quantification: Biological and translational research implications.

Anthony, K; Arechavala-Gomeza, V; Taylor, LE; Vulin, A; Kaminoh, Y; Torelli, S; Feng, L; ... Muntoni, F; + view all (2014) Dystrophin quantification: Biological and translational research implications. Neurology , 83 (22) 2062 - 2069. 10.1212/WNL.0000000000001025. Green open access

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Abstract

We formed a multi-institution collaboration in order to compare dystrophin quantification methods, reach a consensus on the most reliable method, and report its biological significance in the context of clinical trials.

Type: Article
Title: Dystrophin quantification: Biological and translational research implications.
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1212/WNL.0000000000001025
Publisher version: http://dx.doi.org/10.1212/WNL.0000000000001025
Language: English
Additional information: © 2014 American Academy of Neurology This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: Dystrophin, Humans, Medical Laboratory Science, Muscular Dystrophy, Duchenne, Observer Variation, Translational Medical Research
UCL classification: UCL
UCL > Provost and Vice Provost Offices
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 > 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.ucl.ac.uk/id/eprint/1453824
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