Myotonia and muscle contractile properties in mice withSIX5 deficiency
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology
Reference25 articles.
1. Six transcripts map within 200 kilobases of the myotonic dystrophy expanded repeat
2. Myotonic Dystrophy Is Associated with a Reduced Level of RNA from the DMWD Allele Adjacent to the Expanded Repeat
3. DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model
4. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat
5. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
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1. The SIX Family of Transcription Factors: Common Themes Integrating Developmental and Cancer Biology;Frontiers in Cell and Developmental Biology;2021-08-19
2. Gene Therapy and Gene Editing for Myotonic Dystrophy;Muscle Gene Therapy;2019
3. Myotonic dystrophy type 1 (DM1): A triplet repeat expansion disorder;Gene;2013-06
4. Myotonic Dystrophies;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
5. Dynamic Mutations;Advances in Experimental Medicine and Biology;2012
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