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30. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. Mestroni L; Rocco C; Gregori D; Sinagra G; Di Lenarda A; Miocic S; Vatta M; Pinamonti B; Muntoni F; Caforio AL; McKenna WJ; Falaschi A; Giacca M; Camerini J Am Coll Cardiol; 1999 Jul; 34(1):181-90. PubMed ID: 10400009 [TBL] [Abstract][Full Text] [Related]
31. Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study. Brito D; Richard P; Komajda M; Madeira H Rev Port Cardiol; 2008 Feb; 27(2):147-73. PubMed ID: 18488914 [TBL] [Abstract][Full Text] [Related]
32. Familial idiopathic congestive cardiomyopathy in three generations: a family study with eight affected members. MacLennan BA; Tsoi EY; Maguire C; Adgey AA Q J Med; 1987 Apr; 63(240):335-47. PubMed ID: 3685246 [TBL] [Abstract][Full Text] [Related]
33. Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. Villard E; Duboscq-Bidot L; Charron P; Benaiche A; Conraads V; Sylvius N; Komajda M Eur Heart J; 2005 Apr; 26(8):794-803. PubMed ID: 15769782 [TBL] [Abstract][Full Text] [Related]
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