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

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

Balkan Journal of Medical Genetics
Volume 21 (2018): Issue 2 (December 2018)
By: J Finsterer,  C Stöllberger,  A Reining-Festa,  M Loewe-Grgurin and  M Gencik  
Open Access
|Dec 2018
DOI: https://doi.org/10.2478/bjmg-2018-0024 | Journal eISSN: 2199-5761
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Language: English
Page range: 39 - 43
Published on: Dec 31, 2018
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Cardiac involvement,
Creatine kinase (hyper-CKemia),
Multisystem disease,
Myotonia,
Neuromuscular,
gene
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2018 J Finsterer, C Stöllberger, A Reining-Festa, M Loewe-Grgurin, M Gencik, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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