Dystrophin: A clinical perspective
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference89 articles.
1. Muscular dystrophy in an X;1 translocation female suggests that Duchenne locus is on an X chromosome short arm;Lindenbaum;J Med Genet,1979
2. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy;Murray;Nature,1982
3. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome;Davies;Nucleic Acids Res,1983
4. Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome;Franke;Am J Hum Genet,1985
5. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene;Monaco;Nature,1986
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2. Mini-dystrophin efficiently incorporates into the dystrophin protein complex in living cells;Journal of Muscle Research and Cell Motility;2006-02
3. Diagnosis of dystrophinopathy by skin biopsy;Muscle & Nerve;2002-02-19
4. Dynamic restoration of dystrophin to dystrophin-deficient myotubes;Muscle & Nerve;2001-01
5. Introduction;Journal of Pediatric Gastroenterology and Nutrition;1997-07
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