Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD
Author:
Affiliation:
1. Department of Physiology, Anatomy and Genetics, MDUK Oxford Neuromuscular Centre, University of Oxford, Oxford OX1 3PT, United Kingdom
Funder
Medical Research Council
Muscular Dystrophy UK
Summit Therapeutics plc
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddy353/26152369/ddy353.pdf
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3. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene;Monaco;Nature,1986
4. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987
5. The TREAT-NMD DMD global database: analysis of more than 7000 Duchenne muscular dystrophy mutations;Bladen;Hum. Mutat.,2015
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