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Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophy

  • Published:2002-10 Issue: Volume:12 Page:S71-S77
  • ISSN:0960-8966
  • Container-title:Neuromuscular Disorders
  • language:en
  • Short-container-title:Neuromuscular Disorders

Author:

Aartsma-Rus Annemieke,Bremmer-Bout Mattie,Janson Anneke A.M,den Dunnen Johan T,van Ommen Gert-Jan B,van Deutekom Judith C.T

Publisher

Elsevier BV

Subject

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

Reference27 articles.

1. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

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

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

4. The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle;Zubrzycka-Gaarn;Nature,1988

5. Glycoprotein complex anchoring dystrophin to sarcolemma;Yoshida;J Biochem (Tokyo),1990
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