Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://link.springer.com/article/10.1007/s00415-017-8653-2/fulltext.html
Reference36 articles.
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2. Ricker K, Koch MC, Lehmann-Horn F et al (1994) Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts. Neurology 44:1448
3. Liquori CL, Ricker K, Moseley ML et al (2001) Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 293:864–867
4. Suominen T, Bachinski LL, Auvinen S et al (2011) Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland. Eur J Hum Genet 19:776–782
5. Vanacore N, Rastelli E, Antonini G et al (2016) An age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome Province, Italy. Neuroepidemiology 46:191–197
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