Targeting mRNA for the treatment of facioscapulohumeral muscular dystrophy
Author:
Affiliation:
1. Department of Medical Genetics, School of Human Development, Faculty of Medicine and Dentistry, University of Alberta
2. Muscular Dystrophy Canada Research Chair, University of Alberta
Publisher
International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/irdr/5/3/5_2016.01056/_pdf
Reference80 articles.
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2. 2. Deenen JC, Arnts H, van der Maarel SM, Padberg GW, Verschuuren JJ, Bakker E, Weinreich SS, Verbeek AL, van Engelen BG. Population-based incidence and prevalence of facioscapulohumeral dystrophy. Neurology. 2014; 83:1056-1059.
3. 3. Mostacciuolo ML, Pastorello E, Vazza G, Miorin M, Angelini C, Tomelleri G, Galluzzi G, Trevisan CP. Facioscapulohumeral muscular dystrophy: Epidemiological and molecular study in a north-east Italian population sample. Clin Genet. 2009; 75:550-555.
4. 4. Gabriels J, Beckers MC, Ding H, De Vriese A, Plaisance S, van der Maarel SM, Padberg GW, Frants RR, Hewitt JE, Collen D, Belayew A. Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element. Gene. 1999; 236:25-32.
5. 5. Vanderplanck C, Ansseau E, Charron S, Stricwant N, Tassin A, Laoudj-Chenivesse D, Wilton SD, Coppee F, Belayew A. The FSHD atrophic myotube phenotype is caused by DUX4 expression. PloS One. 2011; 6:e26820.
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