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23. Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers. Magagnotti C; Bachi A; Zerbini G; Fattore E; Fermo I; Riba M; Previtali SC; Ferrari M; Andolfo A; Benedetti S Biochim Biophys Acta; 2012 Jun; 1822(6):970-9. PubMed ID: 22326558 [TBL] [Abstract][Full Text] [Related]
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30. Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in LmnaH222P/H222P mutant mice. Wada E; Kato M; Yamashita K; Kokuba H; Liang WC; Bonne G; Hayashi YK PLoS One; 2019; 14(8):e0221512. PubMed ID: 31430335 [TBL] [Abstract][Full Text] [Related]
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33. Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy. Walter MC; Witt TN; Weigel BS; Reilich P; Richard P; Pongratz D; Bonne G; Wehnert MS; Lochmüller H Neuromuscul Disord; 2005 Jan; 15(1):40-4. PubMed ID: 15639119 [TBL] [Abstract][Full Text] [Related]
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