Author:
Asano Jun-ichi,Tomatsu Shunji,Sukegawa Kazuko,Yamaguchi Seiji,Ikedo Yuko,Minami Ryoji,Iida Mitsuo,Nishimura Masaaki,Nakagawa Masanori,Ohshiro Morio,Orii Tadao
Publisher
Springer Science and Business Media LLC
Reference16 articles.
1. Baumbach, L.L., Chamberlain, J.S., Ward, P.A., Farwell, N.J. and Caskey, C.T. 1989. Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies.Neurology
39: 465–474.
2. Burghes, A.H.M., Logan, C., Hu, H., Belfall, B., Worton, R. and Ray, P.N. 1987. Isolation of a cDNA clone from the region of an X;21 translocation that breaks within the Duchenne/Becker muscular dystrophies.Nature
328: 434–437.
3. Darras, B.T., Blattner, P., Harper, J.F., Spiro, A.J., Alter, S. and Francke, U. 1988. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints onHindIII andBglII exoncontaining fragment maps, mitotic origin of the mutations.Am. J. Hum. Genet.
43: 620–629.
4. Forrest, S.M., Cross, G.S., Speer, A., Gardner-Medwin, D., Burnas, J. and Davies, K.E. 1987. Preferential deletion of exons in Duchenne and Becker muscular dystrophies.Nature
329: 638–640.
5. Forrest, S.M., Cross, G.S., Flint, T., Speer, A., Robson, K.J.H. and Davies, K.E. 1988. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.Genomics
2: 109–144.
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