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43. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Muchir A; Bonne G; van der Kooi AJ; van Meegen M; Baas F; Bolhuis PA; de Visser M; Schwartz K Hum Mol Genet; 2000 May; 9(9):1453-9. PubMed ID: 10814726 [TBL] [Abstract][Full Text] [Related]
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56. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation. Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843 [TBL] [Abstract][Full Text] [Related]
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