The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
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Recent Advances in the Molecular Genetics of Familial Hypertrophic Cardiomyopathy in South Asian DescendantsA primer on arrhythmias in patients with hypertrophic cardiomyopathy.Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation.Desensitization of myofilaments to Ca2+ as a therapeutic target for hypertrophic cardiomyopathy with mutations in thin filament proteins.Increased Transforming Growth Factor-β Levels Associated With Cardiac Adverse Events in Hypertrophic Cardiomyopathy.Hypertrophic cardiomyopathy: from mutation to functional analysis of defective protein
P2860
The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
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bilimsel makale
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scientific article published on 15 December 2010
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The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
@en
The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
@nl
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The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
@en
The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
@nl
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The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
@en
The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
@nl
P2093
P2860
P1476
The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
@en
P2093
Albert C van Rossum
Ger J M Stienen
Sabine J van Dijk
Tjeerd Germans
Wessel P Brouwer
P2860
P304
P356
10.1111/J.1365-2362.2010.02439.X
P577
2010-12-15T00:00:00Z