论文信息 - Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy - 字舞流文

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

J. Mogensen | T. Kubo | W. McKenna | A. Shaw | S. Hughes | R. Murphy

[1] J. Mogensen,et al. Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy , 2003, Journal of medical genetics.

[2] P. Elliott,et al. Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations. , 2003, The Journal of clinical investigation.

[3] Towbin Ja,et al. Molecular genetics of left ventricular dysfunction. , 2001 .

[4] L. Mestroni,et al. Clinical StudiesFamilial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity☆ , 1999 .

[5] L. Mestroni,et al. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. , 1999, Journal of the American College of Cardiology.

[6] R. Solaro,et al. Interactions at the NH2-terminal interface of cardiac troponin I modulate myofilament activation. , 1999, Journal of molecular and cellular cardiology.