Wibawa,T, Takeshima,Y, Mitsuyoshi,H., Surono,A, Nakamura,H and Matsuo,M.: "Complete skipping of exon 66 due to novel mutation of the dystrophin gene was identified in two Japanese families of DMD with severe mental retardation"Brain Dev. (in press). (2000
Wibawa,T, Takeshima,Y, Mitsuyoshi,H., Surono,A, Nakamura,H and Matsuo,M.: "Complete skipping of exon 66 due to novel mutation of the dystrophin gene was identified in two Japanese families of DMD with severe mental retardation"Brain Dev. (in press). (2000
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Wibawa,T、Takeshima,Y、Mitsuyoshi,H.、Surono,A、Nakamura,H 和 Matsuo,M.：“由于抗肌营养不良蛋白基因的新突变，在两个患有严重 DMD 的日本家族中发现了外显子 66 的完全跳跃。
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