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7. Human molecular genetics and the elucidation of the primary biochemical defect in Duchenne muscular dystrophy. Hoffman EP Cell Motil Cytoskeleton; 1989; 14(1):163-8. PubMed ID: 2684423 [No Abstract] [Full Text] [Related]
8. An unusual variant of Becker muscular dystrophy. de Visser M; Bakker E; Defesche JC; Bolhuis PA; van Ommen GJ Ann Neurol; 1990 May; 27(5):578-81. PubMed ID: 2193611 [TBL] [Abstract][Full Text] [Related]
18. [The pathogenesis of Duchenne muscular dystrophy--defects of the membrane cytoskeleton "dystrophin"]. Arahata K; Sugita H Nihon Rinsho; 1989 Aug; 47(8):1857-64. PubMed ID: 2685400 [No Abstract] [Full Text] [Related]
19. Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findings. Zatz M; Passos-Bueno MR; Vainzof M; Pavanello RC Am J Med Genet; 1989 Mar; 32(3):438-41. PubMed ID: 2658593 [No Abstract] [Full Text] [Related]
20. The missing link in DMD? Slater CR Nature; 1987 Dec 24-31; 330(6150):693-4. PubMed ID: 3320755 [No Abstract] [Full Text] [Related] [Next] [New Search]