References
- Bulman D E., Gangopadhyay S, Bebchuk K, Worton E, Ray P. Point mutation in the human dystrophin gene: Identification through Western blot analysis. Genomics 1991b; 10: 457–60
- Clerk A, Rodillo E, Heckmatt J, Dubowitz V, Strong P, Sewry C. Characterization of dystrophin in carriers of Duchenne muscular dystrophy. J Neurol Sci 1991; 102: 197–205
- Rowland L. Clinical concepts of Duchenne muscular dystrophy. The impact of molecular genetics. Brain 1988; 111: 479–95
- Boyd Y, Buckle V J. Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy. Clin Genet 1986; 29: 108–15
- Rabbi-Bortolini E, Da Silva D M., Chequer R S., Vianna-Morgante A M., Zatz M. Duchenne muscular dystrophy in a girl with a 45,X/46, XX/47, XXX chromosome constitution. Am J Med Genet 1986b; 25: 239–43
- Beggs A H., Hoffman E P., Snyder J R., Arahata Kiichi, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel L M. Exploring the molecular basis for variability among patients with Becker muscular dystrophy: Dystrophin gene and protein studies. Am J Hum Genet 1991; 49: 54–67
- Nordenskjöld M, Nicholson L, Edstrom L, Anvret M, Eiserman M, Slater C, Stolpe L. A normal male with an inherited deletion of one exon within the DMD gene. Human Genet 1990; 84: 207–9
- Hammonds R. Protein sequence of DMD gene is related to actin binding domain of α-actinin. Cell 1987; 51: 1
- Khurana T S., Watkins S C., Chafey P, Chelly J, Tome F MS, Fardeau M, Kaplan J C., Kunkel L M. Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle. Neuromusc Disord 1991; 1: 185–94
- Love D R., Hill D F., Dickson G, Spurr N K., Byth B C., Marsden R F., Walsh F S., Edwards Y H., Davies K E. An autosomal transcipt in skeletal muscle with homology to dystrophin. Nature 1989; 339: 55–8