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71. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Arimura T; Helbling-Leclerc A; Massart C; Varnous S; Niel F; Lacène E; Fromes Y; Toussaint M; Mura AM; Keller DI; Amthor H; Isnard R; Malissen M; Schwartz K; Bonne G Hum Mol Genet; 2005 Jan; 14(1):155-69. PubMed ID: 15548545 [TBL] [Abstract][Full Text] [Related]
72. Autosomal dominant Emery-Dreifuss dystrophy due to mutations in rod domain of the lamin A/C gene. Felice KJ; Schwartz RC; Brown CA; Leicher CR; Grunnet ML Neurology; 2000 Jul; 55(2):275-80. PubMed ID: 10908904 [TBL] [Abstract][Full Text] [Related]
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78. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration. Bakay M; Wang Z; Melcon G; Schiltz L; Xuan J; Zhao P; Sartorelli V; Seo J; Pegoraro E; Angelini C; Shneiderman B; Escolar D; Chen YW; Winokur ST; Pachman LM; Fan C; Mandler R; Nevo Y; Gordon E; Zhu Y; Dong Y; Wang Y; Hoffman EP Brain; 2006 Apr; 129(Pt 4):996-1013. PubMed ID: 16478798 [TBL] [Abstract][Full Text] [Related]
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