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Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides

  • Published:1999-07 Issue:5 Volume:9 Page:330-338
  • ISSN:0960-8966
  • Container-title:Neuromuscular Disorders
  • language:en
  • Short-container-title:Neuromuscular Disorders

Author:

Wilton Stephen D,Lloyd Frances,Carville Kylie,Fletcher Sue,Honeyman Kaite,Agrawal Sudhir,Kole Ryszard

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference39 articles.

1. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion;Koenig;Am J Hum Genet,1989

2. An explanation for the phenotypic differences between patients bearing partial deletions of the dmd locus;Monaco;Genomics,1988

3. X chromosome-linked muscular dystrophy (mdx) in the mouse;Bulfield;Proc Natl Acad Sci USA,1984

4. Myoblast transfer: a possible therapy for inherited myopathies?;Partridge;Muscle Nerve,1991

5. Cell and gene therapy in Duchenne muscular dystrophy;Morgan;Hum Gene Ther,1994
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