A. Aartsma-rus, A. Janson, W. Kaman, M. Bremmer-bout, G. Van-ommen et al., Antisense-Induced Multiexon Skipping for Duchenne Muscular Dystrophy Makes More Sense, The American Journal of Human Genetics, vol.74, issue.1, pp.83-92, 2004.
DOI : 10.1086/381039

A. Aartsma-rus, W. Kaman, M. Bremmer-bout, A. Janson, J. Den-dunnen et al., Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells, Gene Therapy, vol.11, issue.18, pp.1391-1398, 2004.
DOI : 10.1038/sj.gt.3302313

L. Anderson and K. Davison, Multiplex Western Blotting System for the Analysis of Muscular Dystrophy Proteins, The American Journal of Pathology, vol.154, issue.4, pp.1017-1022, 1999.
DOI : 10.1016/S0002-9440(10)65354-0

A. Beggs, E. Hoffman, J. Snyder, K. Arahata, L. Specht et al., Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies, Am J Hum Genet, vol.49, pp.54-67, 1991.

C. Beroud, G. Collod-beroud, C. Boileau, T. Soussi, and C. Junien, UMD (Universal Mutation Database): A generic software to build and analyze locus-specific databases, Human Mutation, vol.3, issue.1, pp.86-94, 2000.
DOI : 10.1002/(SICI)1098-1004(200001)15:1<86::AID-HUMU16>3.0.CO;2-4
URL : https://hal.archives-ouvertes.fr/inserm-00143606

C. Beroud, D. Hamroun, G. Collod-beroud, C. Boileau, T. Soussi et al., UMD (Universal Mutation Database): 2005 update, ): 2005 update, pp.184-191, 2005.
DOI : 10.1002/humu.20210
URL : https://hal.archives-ouvertes.fr/inserm-00143605

A. Bornemann and L. Anderson, Diagnostic Protein Expression in Human Muscle Biopsies, Brain Pathology, vol.17, issue.2, pp.193-214, 2000.
DOI : 10.1111/j.1750-3639.2000.tb00254.x

L. Cartegni, J. Wang, Z. Zhu, M. Zhang, and A. Krainer, ESEfinder: a web resource to identify exonic splicing enhancers, Nucleic Acids Research, vol.31, issue.13, pp.3568-3571, 2003.
DOI : 10.1093/nar/gkg616

G. Crawford, Q. Lu, T. Partridge, and J. Chamberlain, Suppression of revertant fibers in mdx mice by expression of a functional dystrophin, Human Molecular Genetics, vol.10, issue.24, pp.2745-2750, 2001.
DOI : 10.1093/hmg/10.24.2745

E. Fabbrizio, J. Leger, M. Anoal, J. Leger, and D. Mornet, Monoclonal antibodies targeted against the C-terminal domain of dystrophin or utrophin, FEBS Letters, vol.3, issue.1, pp.10-14, 1993.
DOI : 10.1016/0014-5793(93)81100-E

W. Fairbrother, G. Yeo, R. Yeh, P. Goldstein, M. Mawson et al., RESCUE-ESE identifies candidate exonic splicing enhancers in vertebrate exons, Nucleic Acids Research, vol.32, issue.Web Server, pp.187-190, 2004.
DOI : 10.1093/nar/gkh393

A. Fall, R. Johnsen, K. Honeyman, P. Iversen, S. Fletcher et al., Induction of revertant fibres in the mdx mouse using antisense oligonucleotides, Genetic Vaccines and Therapy, vol.4, issue.1, p.3, 2006.
DOI : 10.1186/1479-0556-4-3

I. Fokkema, J. Den-dunnen, and P. Taschner, LOVD: Easy creation of a locus-specific sequence variation database using an ???LSDB-in-a-box??? approach, Human Mutation, vol.21, issue.2, pp.63-68, 2005.
DOI : 10.1002/humu.20201

A. Goyenvalle, A. Vulin, F. Fougerousse, F. Leturcq, J. Kaplan et al., Rescue of Dystrophic Muscle Through U7 snRNA-Mediated Exon Skipping, Science, vol.306, issue.5702, pp.1796-1799, 2004.
DOI : 10.1126/science.1104297

A. Herczegfalvi, G. Toth, P. Gyurus, E. Morava, E. Endreffy et al., Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies, Neuromuscular Disorders, vol.9, issue.8, pp.552-554, 1999.
DOI : 10.1016/S0960-8966(99)00044-9

E. Hoffman, R. Brown, . Jr, and L. Kunkel, Dystrophin: The protein product of the duchenne muscular dystrophy locus, Cell, vol.51, issue.6, pp.919-928, 1987.
DOI : 10.1016/0092-8674(87)90579-4

R. Kapsa, A. Kornberg, and E. Byrne, Novel therapies for Duchenne muscular dystrophy, The Lancet Neurology, vol.2, issue.5, pp.299-310, 2003.
DOI : 10.1016/S1474-4422(03)00382-X

G. Kobinger, J. Louboutin, E. Barton, H. Sweeney, and J. Wilson, Targeting of Muscle Progenitor Cells, Human Gene Therapy, vol.14, issue.15, pp.1441-1449, 2003.
DOI : 10.1089/104303403769211655

M. Koenig, E. Hoffman, C. Bertelson, A. Monaco, C. Feener et al., Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals, Cell, vol.50, issue.3, pp.509-517, 1987.
DOI : 10.1016/0092-8674(87)90504-6

M. Koenig, A. Monaco, and L. Kunkel, The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein, Cell, vol.53, issue.2, pp.219-226, 1988.
DOI : 10.1016/0092-8674(88)90383-2

M. Koenig, A. Beggs, M. Moyer, S. Scherpf, K. Heindrich et al., The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion, Am J Hum Genet, vol.45, pp.498-506, 1989.

U. Lenk, S. Demuth, U. Kraft, R. Hanke, and A. Speer, Alternative splicing of dystrophin mRNA complicates carrier determination: report of a DMD family., Journal of Medical Genetics, vol.30, issue.3, pp.206-209, 1993.
DOI : 10.1136/jmg.30.3.206

S. Li, E. Kimura, B. Fall, M. Reyes, J. Angello et al., Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin, Gene Therapy, vol.101, issue.14, pp.1099-1108, 2005.
DOI : 10.1038/sj.gt.3302505

Q. Lu, A. Rabinowitz, Y. Chen, T. Yokota, H. Yin et al., Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles, Proceedings of the National Academy of Sciences, vol.102, issue.1, pp.198-203, 2005.
DOI : 10.1073/pnas.0406700102

A. Monaco, C. Bertelson, S. Liechti-gallati, H. Moser, and L. Kunkel, An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus, Genomics, vol.2, issue.1, pp.90-95, 1988.
DOI : 10.1016/0888-7543(88)90113-9

A. Morrone, E. Zammarchi, P. Scacheri, M. Donati, R. Hoop et al., Asymptomatic dystrophinopathy, American Journal of Medical Genetics, vol.27, issue.3, pp.261-267, 1997.
DOI : 10.1002/(SICI)1096-8628(19970331)69:3<261::AID-AJMG9>3.0.CO;2-O

I. Nonaka, [Muscular dystrophy: advances in research works and therapeutic trials], Rinsho Shinkeigaku, vol.44, pp.901-904, 2004.

S. Phelps, M. Hauser, N. Cole, J. Rafael, R. Hinkle et al., mice, Human Molecular Genetics, vol.4, issue.8, pp.1251-1258, 1995.
DOI : 10.1093/hmg/4.8.1251

M. Sironi, A. Bardoni, G. Felisari, R. Cagliani, M. Robotti et al., Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle, Journal of the Neurological Sciences, vol.186, issue.1-2, pp.51-57, 2001.
DOI : 10.1016/S0022-510X(01)00502-0

M. Sironi, G. Menozzi, L. Riva, R. Cagliani, G. Comi et al., Silencer elements as possible inhibitors of pseudoexon splicing, Nucleic Acids Research, vol.32, issue.5, pp.1783-1791, 2004.
DOI : 10.1093/nar/gkh341

A. Surono, T. Van-khanh, Y. Takeshima, H. Wada, M. Yagi et al., Chimeric RNA/Ethylene-Bridged Nucleic Acids Promote Dystrophin Expression in Myocytes of Duchenne Muscular Dystrophy by Inducing Skipping of the Nonsense Mutation-Encoding Exon, Human Gene Therapy, vol.15, issue.8, pp.749-757, 2004.
DOI : 10.1089/1043034041648444

S. Takeda, [Current status and perspective of gene therapy on dystrophic animal model], Rinsho Shinkeigaku, vol.44, pp.911-913, 2004.

Z. Wang, M. Rolish, G. Yeo, V. Tung, M. Mawson et al., Systematic Identification and Analysis of Exonic Splicing Silencers, Cell, vol.119, issue.6, pp.831-845, 2004.
DOI : 10.1016/j.cell.2004.11.010

S. Wilton, D. Dye, and N. Laing, Dystrophin gene transcripts skipping the mdx mutation, Muscle & Nerve, vol.46, issue.6, pp.728-734, 1997.
DOI : 10.1002/(SICI)1097-4598(199706)20:6<728::AID-MUS10>3.0.CO;2-Q

M. Yoshimura, M. Sakamoto, M. Ikemoto, Y. Mochizuki, K. Yuasa et al., AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype, Molecular Therapy, vol.10, issue.5, pp.821-828, 2004.
DOI : 10.1016/j.ymthe.2004.07.025

X. Zhang and L. Chasin, Computational definition of sequence motifs governing constitutive exon splicing, Genes & Development, vol.18, issue.11, pp.1241-1250, 2004.
DOI : 10.1101/gad.1195304