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1 iciency is probably the most common cause of familial dilated cardiomyopathy.
2 2 different SCN5A mutations associated with familial dilated cardiomyopathy.
3 ), which has previously been associated with familial dilated cardiomyopathy.
4 study is to identify novel mutations causing familial dilated cardiomyopathy.
5 proteins have been recorded in patients with familial dilated cardiomyopathy.
6 aluations were performed in 21 kindreds with familial dilated cardiomyopathy.
7 lioma, split-hand/foot deformity type 1, and familial dilated cardiomyopathy.
8 e, familial hypertrophic cardiomyopathy, and familial dilated cardiomyopathy.
9 unt for approximately 10 percent of cases of familial dilated cardiomyopathy and are particularly pre
10 lament-Ca(2)(+) responsiveness in a model of familial dilated cardiomyopathy and improve cardiac func
15 and that two lamin A mutants associated with familial dilated cardiomyopathy, E203G and E203K, exhibi
16 imed to characterize the clinical profile of familial dilated cardiomyopathy (FDC) in the families of
18 ted cardiomyopathy occurring in families, or familial dilated cardiomyopathy (FDC), may occur in 20%
22 arch comparing the survival of children with familial dilated cardiomyopathy (FDCM) to that of childr
26 fy the causal variant in a large family with familial dilated cardiomyopathy of unknown pathogenesis.
27 ecause of prominent genetic heterogeneity in familial dilated cardiomyopathy, recognition of pathogen
28 S for mutations in 116 DCM families from the Familial Dilated Cardiomyopathy Registry and in 309 subj
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