Author:
Dwianingsih Ery Kus,Malueka Rusdy Ghazali,Nishida Atsushi,Itoh Kyoko,Lee Tomoko,Yagi Mariko,Iijima Kazumoto,Takeshima Yasuhiro,Matsuo Masafumi
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference43 articles.
1. Monaco, A. P., Bertelson, C. J., Liechti-Gallati, S., Moser, H. & Kunkel, L. M. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics 2, 90–95 (1988).
2. Beggs, A. H., Koenig, M., Boyce, F. M. & Kunkel, L. M. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum. Genet. 86, 45–48 (1990).
3. Tuffery-Giraud, S., Beroud, C., Leturcq, F., Yaou, R. B., Hamroun, D., Michel-Calemard, L. et al. Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase. Hum. Mutat. 30, 934–945 (2009).
4. Koenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T. et al. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Am. J. Hum. Genet. 45, 498–506 (1989).
5. Kesari, A., Pirra, L., Bremadesam, L., McIntyre, O., Gordon, E., Dubrovsky, A. et al. Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule. Hum. Mutat. 17, 728–737 (2008).
Cited by
29 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献