The hallmarks of myotonic dystrophy type 1 muscle dysfunction-Reference-Cited by-同舟云学术

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The hallmarks of myotonic dystrophy type 1 muscle dysfunction

Published:2020-12-02 Issue:2 Volume:96 Page:716-730
ISSN:1464-7931
Container-title:Biological Reviews
language:en
Short-container-title:Biol Rev

Author:

Ozimski Lauren L.¹²³⁴,Sabater‐Arcis Maria¹²³,Bargiela Ariadna¹²³^ORCID,Artero Ruben¹²³^ORCID

Affiliation:

1. Translational Genomics Group Incliva Health Research Institute Avda. Menéndez Pelayo 4 acc. Valencia 46010 Spain

2. University Institute for Biotechnology and Biomedicine Dr. Moliner 50 Burjasot Valencia 46100 Spain

3. CIPF‐INCLIVA Joint Unit Valencia 46012 Spain

4. Arthex Biotech Catedrático Escardino, 9 Paterna Valencia 46980 Spain

Funder

Generalitat Valenciana

Ministerio de Ciencia e Innovación

Publisher

Wiley

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/brv.12674

Reference101 articles.

1. Myogenic defects in myotonic dystrophy

2. Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds

3. ThemuscleblindGene Participates in the Organization of Z-Bands and Epidermal Attachments ofDrosophilaMuscles and Is Regulated byDmef2

4. Consensus-based care recommendations for adults with myotonic dystrophy type 1

5. Altered MEF2 isoforms in myotonic dystrophy and other neuromuscular disorders

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