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Genetic Diagnosis of Duchenne and Becker Muscular Dystrophy using Multiplex Ligation-Dependent Probe Amplification in Rwandan Patients

✍ Scribed by Uwineza, A.; Hitayezu, J.; Murorunkwere, S.; Ndinkabandi, J.; Kalala Malu, C. K.; Caberg, J. H.; Dideberg, V.; Bours, V.; Mutesa, L.

Book ID: 124170713
Publisher: Oxford University Press
Year: 2013
Tongue: English
Weight: 642 KB
Volume: 60
Category: Article
ISSN: 0142-6338
DOI: 10.1093/tropej/fmt090

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