Duchenne's Muscular Dystrophy: Review and Recent Scientific Findings
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference48 articles.
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2. Muscular dystrophy in girls with X; autosome translocations;Boyd;J Med Genet,1986
3. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome;Verellen-Dumoulin;Hum Genet,1984
4. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion;Kunkel;Proc Natl Acad Sci USA,1985
5. Cloning the gene for an inherited human disorder-chronic granulomatous disease-on the basis of its chromosomal location;Royer-Pokora;Nature,1986
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1. Duchenne Muscular Dystrophy: Prevalence and patterns of cardiac involvement;The Indian Journal of Pediatrics;2005-05
2. Proteomic method detects oxidatively induced protein carbonyls in muscles of a diabetes model Otsuka Long-evans Tokushima Fatty (OLETF) rat;Free Radical Biology and Medicine;2003-01
3. Separation techniques for high-molecular-mass proteins;Journal of Chromatography B;2002-05
4. Skeletal, cardiac, and smooth muscle failure in Duchenne muscular dystrophy;Pediatric Neurology;1996-01
5. Immunohistochemical analysis of the distribution of MyoD1 in muscle biopsies of primary myopathies and neurogenic atrophy;Acta Neuropathologica;1994-06
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