Author:
HAGHSHENAS MARYAM,AKBARI MOHAMMAD TAGHI,KARIZI SHOHREH ZARE,DEILAMANI FARAVAREH KHORDADPOOR,NAFISSI SHAHRIAR,SALEHI ZIVAR
Publisher
Springer Science and Business Media LLC
Reference23 articles.
1. Almomani R., van der Stoep N., Bakker E., den Dunnen J. T., Breuning, M. H. and Ginjaar I. B. 2009 Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis. Neuromuscul. Disord. 19, 383–390.
2. Bushby K., Finkel R., Birnkrant D. J., Case L. E., Clemens P. R., Cripe L. et al. 2010 Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care. Lancet Neurol. 9, 177–189.
3. Campbell K. P. 1995 Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. Cell 80, 675–679.
4. Chen W. J., Lin Q. F., Zhang Q. J., He J., Liu X. Y., Lin M. T. et al. 2013 Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing. Clin. Chim. Acta 423, 35–38.
5. Den Dunnen J. T., Grootscholten P. M., Bakker E., Blonden L. A., Ginjaar H. B., Wapenaar M. C. et al. 1989 Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Am. J. Hum. Genet. 45, 835–847.
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