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

✍ Scribed by M. Sironi; S. Corti; F. Locatelli; R. Cagliani; G.P. Comi

Publisher: John Wiley and Sons
Year: 2001
Tongue: English
Weight: 12 KB
Volume: 17
Category: Article
ISSN: 1059-7794
DOI: 10.1002/humu.18

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