Myotonic dystrophy: approach to therapy-Reference-Cited by-同舟云学术

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Myotonic dystrophy: approach to therapy

Published:2017-06 Issue: Volume:44 Page:135-140
ISSN:0959-437X
Container-title:Current Opinion in Genetics & Development
language:en
Short-container-title:Current Opinion in Genetics & Development

Author:

Thornton Charles A,Wang Eric,Carrell Ellie M

Funder

National Institutes of Health

Muscular Dystrophy Association

Myotonic Dystrophy Foundation

Publisher

Elsevier BV

Subject

Developmental Biology,Genetics

Reference65 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;Cell,1992

2. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9;Liquori;Science,2001

3. RNA-mediated neurodegeneration in repeat expansion disorders;Todd;Ann Neurol,2010

4. Developmental expression of mouse muscleblind genes Mbnl1, Mbnl2 and Mbnl3;Kanadia;Gene Expr Patterns,2003

5. MBNL binds similar RNA structures in the CUG repeats of myotonic dystrophy and its pre-mRNA substrate cardiac troponin T;Warf;RNA,2007

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