Concepedia

Myotonic Dystrophy Type 2 – Data from the Serbian Registry

Ivo Božović, Stojan Perić, Jovan Pešović, Bogdan Bjelica, Miloš Brkušanin, Ivana Basta, Marija Božić, Ivan Senćanić, Ana Marjanović, Marija Branković,

Journal of Neuromuscular Diseases · 2018 · 15 citations · 22 references

DOI

Abstract

This registry offers a spectrum of different features presented in Serbian DM2 population, which could be at service of earlier diagnosis and better treatment.

References

22

Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of <i>ZNF9</i>

Christina L. Liquori, K. Ricker, Melinda L. Moseley et al. · Science · 2001 · 1.2K citations

Interobserver agreement in the assessment of muscle strength and functional abilities in Guillain‐Barré syndrome

R. P. Kleyweg, F.G.A. van der Meché, Paul Schmitz · Muscle & Nerve · 1991 · 885 citations

Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1

William J. Groh, Miriam R. Groh, Chandan Saha et al. · New England Journal of Medicine · 2008 · 504 citations · Full text

Myotonic dystrophy type 2

John Day, K. Ricker, Jennifer F. Jacobsen et al. · Neurology · 2003 · 456 citations

Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland

Tiina Suominen, Linda L. Bachinski, S. Auvinen et al. · European Journal of Human Genetics · 2011 · 134 citations · Full text

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