Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues-Reference-Cited by-同舟云学术

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Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues

Published:2010-11-01 Issue:1 Volume:20 Page:1-15
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

López Castel Arturo,Nakamori Masayuki,Tomé Stephanie,Chitayat David,Gourdon Geneviève,Thornton Charles A.,Pearson Christopher E.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/20/1/1/17251411/ddq427.pdf

Reference104 articles.

1. Clinical and molecular aspects of the myotonic dystrophies: a review;Machuca-Tzili;Muscle Nerve,2005

2. Myotonic dystrophies type 1 and 2: a summary on current aspects;Schara;Semin. Pediatr. Neurol.,2006

3. Repeat instability as the basis for human diseases and as a potential target for therapy;López Castel;Nat. Rev. Mol. CellBiol.,2010

4. RNA-mediated neuromuscular disorders;Ranum;Annu. Rev. Neurosci.,2006

5. Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP;Klesert;Nat. Genet.,1997

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