Evaluation of serum MMP-9 as predictive biomarker for antisense therapy in Duchenne
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-17982-y.pdf
Reference42 articles.
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2. Helderman-van den Enden, A. T. J. M. et al. An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy. Eur. J. Hum. Genet. 1–6 https://doi.org/10.1038/ejhg.2012.101 (2012).
3. van den Bergen, J. C. et al. Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapy. J. Neurol. Neurosurg. Psychiatry 85, 92–8 (2014).
4. Henricson, E. K. et al. Thecooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and othe. Muscle Nerve 48, 55–67 (2013).
5. Aartsma-Rus, A. Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients. Hum. Mol. Genet. 12, 907–914 (2003).
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