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2. The childhood muscular dystrophies: making order out of chaos. Tsao CY; Mendell JR Semin Neurol; 1999; 19(1):9-23. PubMed ID: 10711985 [TBL] [Abstract][Full Text] [Related]
3. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Ervasti JM; Ohlendieck K; Kahl SD; Gaver MG; Campbell KP Nature; 1990 May; 345(6273):315-9. PubMed ID: 2188135 [TBL] [Abstract][Full Text] [Related]
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9. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries. Fardeau M; Matsumura K; Tomé FM; Collin H; Leturcq F; Kaplan JC; Campbell KP C R Acad Sci III; 1993 Aug; 316(8):799-804. PubMed ID: 8044705 [TBL] [Abstract][Full Text] [Related]
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11. Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR. Arning L; Jagiello P; Schara U; Vorgerd M; Dahmen N; Gencikova A; Mortier W; Epplen JT; Gencik M J Neurol; 2004 Jan; 251(1):72-8. PubMed ID: 14999492 [TBL] [Abstract][Full Text] [Related]
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14. Common pathological mechanisms in mouse models for muscular dystrophies. Turk R; Sterrenburg E; van der Wees CG; de Meijer EJ; de Menezes RX; Groh S; Campbell KP; Noguchi S; van Ommen GJ; den Dunnen JT; 't Hoen PA FASEB J; 2006 Jan; 20(1):127-9. PubMed ID: 16306063 [TBL] [Abstract][Full Text] [Related]
15. Dystrophin assay in muscular dystrophies: an Indian experience. Jain S; Sarkar C; Dinda AK; Maheshwari MC Natl Med J India; 1993; 6(6):259-62. PubMed ID: 7950930 [TBL] [Abstract][Full Text] [Related]
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17. A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex. MacLeod H; Pytel P; Wollmann R; Chelmicka-Schorr E; Silver K; Anderson RB; Waggoner D; McNally EM Neuromuscul Disord; 2007 Apr; 17(4):285-9. PubMed ID: 17336067 [TBL] [Abstract][Full Text] [Related]
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