Hagiwara Y.,1994
Hagiwara Y., Nishio H., Kitoh Y., Takeshima Y., Narita N., Wada H., Yokoyama M., Nakamura H., Matsuo M. A novel point mutation (G(-1) to T) in a 5-prime splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy. - Am.J.Hum. Genet., 1994, v. 54, p. 53-61.
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