2017
DOI: 10.1101/gad.302893.117
|View full text |Cite
|
Sign up to set email alerts
|

Congenital myotonic dystrophy—an RNA-mediated disease across a developmental continuum

Abstract: Thomas and colleagues (pp. 1122-1133) demonstrate severe dysregulation of developmentally regulated alternative splicing and polyadenylation in congenital myotonic dystrophy (CDM). In doing so, they also highlight the importance of these post-transcriptional processes during normal fetal muscle development. Finally, they generate and characterize a mouse model of CDM that lacks all three Muscleblind-like proteins.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Year Published

2021
2021
2021
2021

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
references
References 10 publications
(16 reference statements)
0
0
0
Order By: Relevance