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Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion
- Correspondence to: Dr A Ferlini, Dipartimento di Medicina Sperimentale e Diagnostica-Sezione di Genetica Medica, Università di Ferrara, Via L Borsari 46, 44100 Ferrara, Italy; fla{at}unife.it
Citation
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion
Publication history
- First published August 14, 2003.
Online issue publication
April 27, 2016
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Copyright 2003 Journal of Medical Genetics