Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype-Reference-Cited by-同舟云学术

Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype

Published:2022-12-22 Issue:2 Volume:67 Page:130-137
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle and Nerve

Author:

Joosten Isis B.T.¹^ORCID,Horlings Corinne G. C.¹²,Vosse Bettine A. H.³^ORCID,Wagner Anouk¹,Bovenkerk David S. H.¹,Evertz Reinder⁴,Vernooy Kevin⁴⁵^ORCID,van Engelen Baziel G. M.⁶^ORCID,Faber Catharina G.¹^ORCID

Affiliation:

1. Department of Neurology and School for Mental Health and Neuroscience Maastricht University Medical Centre+ Maastricht The Netherlands

2. Department of Neurology Medical University Innsbruck Innsbruck Austria

3. Department of Respiratory Medicine Maastricht University Medical Centre+ Maastricht The Netherlands

4. Department of Cardiology Radboud University Medical Centre Nijmegen The Netherlands

5. Department of Cardiology Cardiovascular Research Institute Maastricht, Maastricht University Medical Centre+ Maastricht The Netherlands

6. Department of Neurology Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Centre Nijmegen The Netherlands

Funder

Prinses Beatrix Spierfonds

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.27766

Reference34 articles.

1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook JD;Cell,1992

2. Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2

3. Myotonic dystrophy

4. Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms

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