Technology Insight: therapy for Duchenne muscular dystrophy—an opportunity for personalized medicine?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology
Link
http://www.nature.com/articles/ncpneuro0737.pdf
Reference82 articles.
1. Emery A and Muntoni F (2003) Duchenne Muscular Dystrophy, edn 3. New York: Oxford University Press
2. Nigro G et al. (1983) Prospective study of X-linked progressive muscular dystrophy in Campania. Muscle Nerve 6: 253–262
3. Online Mendelian Inheritance in Man, OMIM® (2006) Johns Hopkins University, Baltimore, MD. OMIM® number: 300376 [ http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300376 ]
4. Koenig M et al. (1987) Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50: 509–517
5. Hoffman EP et al. (1987) Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51: 919–928
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