6Monaco AP, Bertelson C J, Liechti-Gallati S, et al. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus [J].Genomics, 1988,2(1):90-95.
7Winnard AV, Mendell JR, Prior TW, et al. Frameshift deletions ofexons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production [J]. Am J Hum Genet, 1995,56(1): 158-166.
8Gangopadhyay SB, Sherratt TG, Heckmatt JZ, et al. Dystrophin in frameshift deletion patients with Becker muscular dystrophy [J]. Am J Hum Genet, 1992, 51 (3):562-570.
9Gualandi F, Rimerssi p, Rimessi P, Trabanelli C, et al. Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5'mutation hot spot of the dystrophin gene [J]. Gene, 2006, 370(2006): 26-33.
10Chelly J, Gilgenkrantz H, Lambert M, et al. Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies [J]. Cell, 1990, 63(6): 1239-1248.