☆ 4.5 Article

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

HUMAN MUTATION (2001)

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Journal

HUMAN MUTATION
Volume 17, Issue 3, Pages 239-239

Publisher

WILEY-LISS
DOI: 10.1002/humu.18

Keywords

dystrophin; DMD; splicing

Categories

Genetics & Heredity

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