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

.blurhash-client-img { display: none !important; }

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

Authors

J Finsterer

fifigs1@yahoo.de

Krankenanstalt Rudolfstiftung, Messerli Institute, Veterinary University of Vienna, Vienna, Austria

C Stöllberger

Department of Neurology, Krankenanstalt Rudolfstiftung, Vienna, Austria

A Reining-Festa

Neurological Department, Krankenanstalt Rudolfstiftung, Vienna, Austria

M Loewe-Grgurin

Radiological Department, Krankenanstalt Rudolfstiftung, Vienna, Austria

M Gencik

Laboratory for Human Genetics, Vienna, Austria

DOI: https://doi.org/10.2478/bjmg-2018-0024 | Journal eISSN: 2199-5761

Journal RSS Feed

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,

Related subjects:

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.

Previous article Volume 21 (2018): Issue 2 (December 2018)Next article