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23. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. Fatkin D; MacRae C; Sasaki T; Wolff MR; Porcu M; Frenneaux M; Atherton J; Vidaillet HJ; Spudich S; De Girolami U; Seidman JG; Seidman C; Muntoni F; Müehle G; Johnson W; McDonough B N Engl J Med; 1999 Dec; 341(23):1715-24. PubMed ID: 10580070 [TBL] [Abstract][Full Text] [Related]
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29. A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement. van der Kooi AJ; Ledderhof TM; de Voogt WG; Res CJ; Bouwsma G; Troost D; Busch HF; Becker AE; de Visser M Ann Neurol; 1996 May; 39(5):636-42. PubMed ID: 8619549 [TBL] [Abstract][Full Text] [Related]
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