Hagiwara, Y., Nishio, H., Kitoh, Y., Takeshima, Y., Narita, N., Wada, H., . . . Matsuo, M. (1994). A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.

Hagiwara, Y., H. Nishio, Y. Kitoh, Y. Takeshima, N. Narita, H. Wada, M. Yokoyama, H. Nakamura, and M. Matsuo. A Novel Point Mutation (G-1 to T) in a 5' Splice Donor Site of Intron 13 of the Dystrophin Gene Results in Exon Skipping and Is Responsible for Becker Muscular Dystrophy. 1994.

Hagiwara, Y., et al. A Novel Point Mutation (G-1 to T) in a 5' Splice Donor Site of Intron 13 of the Dystrophin Gene Results in Exon Skipping and Is Responsible for Becker Muscular Dystrophy. 1994.