Spinal Muscular Atrophy Therapeutics: Where do we Stand?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Clinical Neurology,Pharmacology
Link
http://link.springer.com/content/pdf/10.1007/s13311-015-0337-y.pdf
Reference112 articles.
1. Werdnig G. Zwei fruhinfantile heriditare Falle von progressiver Muskelatrophie unter dem Bilde der Dystrophie, aber auf neurotischer Grundlage. Arch Psychiatr Nervenkr, 1891.
2. Hoffmann J. Ueber chronische spinale Muskelatrophie im Kindesalter, auf familiärer Basis. Deutsche Zeitschrift f. Nervenheilkunde 1893;3:427-470.
3. Ogino S, Leonard DGB, Rennert H, Ewens WJ, Wilson RB. Genetic risk assessment in carrier testing for spinal muscular atrophy. Am J Med Genet 2002;110:301-307.
4. Prior TW, Snyder PJ, Rink BD, et al. Newborn and carrier screening for spinal muscular atrophy. Am J Med Genet 2010;152A:1608-1616.
5. Lunn MR, Wang CH. Spinal muscular atrophy. Lancet 2008;371:2120-2133.
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