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Citation: T. Wibawa et al., Complete skipping of exon 66 due to novel mutations of the dystrophin genewas identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation, BRAIN DEVEL, 22(2), 2000, pp. 107-112

Authors: Pramono, ZAD Takeshima, Y Surono, A Ishida, T Matsuo, M

Citation: Zad. Pramono et al., A novel cryptic exon in intron 2 of the human dystrophin gene evolved froman intron by acquiring consensus sequences for splicing at different stages of anthropoid evolution, BIOC BIOP R, 267(1), 2000, pp. 321-328

Authors: Surono, A Takeshima, Y Wibawa, T Ikezawa, M Nonaka, I Matsuo, M

Citation: A. Surono et al., Circular dystrophin RNAs consisting of exons that were skipped by alternative splicing, HUM MOL GEN, 8(3), 1999, pp. 493-500