UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion

Gualandi, F and Trabanelli, C and Rimessi, P and Calzolari, E and Toffolatti, L and Patarnello, T and Kunz, G and Muntoni, F and Ferlini, A (2003) Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. J MED GENET , 40 (8) , Article e100.

Full text not available from this repository.


Type:Article
Title:Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion
Keywords:BECKER MUSCULAR-DYSTROPHY, LINKED DILATED CARDIOMYOPATHY, ACTIN-BINDING DOMAIN, SPLICING SILENCER, FRAMESHIFT DELETIONS, SKELETAL-MUSCLE, MESSENGER-RNA, GENE, DUCHENNE, TRANSCRIPTS
UCL classification:UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Child Health > Department of Neurosciences and Mental Health > ICH - Dubowitz Neuromuscular Centre

Archive Staff Only: edit this record