A novel splice site mutation (3157+1G > T) in the dystrophin gene causing total exon skipping and DMD phenotype

A novel splice site mutation (3157+1G > T) in the dystrophin gene causing total exon skipping and DMD phenotype / M. Sironi, S. Corti, F. Locatelli, R. Cagliani, G. Comi. - In: HUMAN MUTATION. - ISSN 1059-7794. - 17:3(2001), pp. 239-239.