Recent Advances in Myotonic Dystrophy Type 2
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Neuroscience
Link
http://link.springer.com/content/pdf/10.1007/s11910-013-0429-1.pdf
Reference48 articles.
1. Liquori CL et al. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science. 2001;293(5531):864–7.
2. Thornton CA, Griggs RC, Moxley 3rd RT. Myotonic dystrophy with no trinucleotide repeat expansion. Ann Neurol. 1994;35(3):269–72.
3. Ricker K et al. Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy. Arch Neurol. 1995;52(1):25–31.
4. Rowland LP. Thornton-Griggs-Moxley disease: myotonic dystrophy type 2. Ann Neurol. 1994;36(5):803–4.
5. Ricker K et al. Linkage of proximal myotonic myopathy to chromosome 3q. Neurology. 1999;52(1):170–1.
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