Myotonic dystrophy-2: Unusual phenotype due to a small CCTG-expansion

Article Category: Case Report

Data publikacji: 31 gru 2018

Zakres stron: 39 - 43

DOI: https://doi.org/10.2478/bjmg-2018-0024

Słowa kluczowe

Cardiac involvement, Creatine kinase (hyper-CKemia), Multisystem disease, Myotonia, Neuromuscular, gene

© 2018 Finsterer J, Stöllberger C, Reining-Festa A, Loewe-Grgurin M, Gencik M, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.