Pages that link to "Q48076472"

The following pages link to Deletion in TNNI3 gene is associated with restrictive cardiomyopathy. (Q48076472):

Displaying 15 items.

• Cardiac troponin mutations and restrictive cardiomyopathy (Q21328674) (← links)
• Calcium-regulated conformational change in the C-terminal end segment of troponin I and its binding to tropomyosin (Q28243781) (← links)
• Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function? (Q28264798) (← links)
• Genotype-specific pathogenic effects in human dilated cardiomyopathy. (Q33903336) (← links)
• Fetal cardiac troponin isoforms rescue the increased Ca2 sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach (Q35063399) (← links)
• Application of echocardiography on transgenic mice with cardiomyopathies (Q35998107) (← links)
• Insights into restrictive cardiomyopathy from clinical and animal studies (Q36077266) (← links)
• Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing (Q36143047) (← links)
• Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology (Q36954073) (← links)
• The functional significance of the last 5 residues of the C-terminus of cardiac troponin I. (Q36984498) (← links)
• Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all (Q37255253) (← links)
• Pediatric restrictive cardiomyopathy due to a heterozygous mutation of the TNNI3 gene (Q41895200) (← links)
• Structural consequences of mutations associated with idiopathic restrictive cardiomyopathy (Q47918639) (← links)
• Restrictive Cardiomyopathy or Constrictive Pericarditis: An Unresolved Conundrum (Q49544866) (← links)
• Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology (Q62476511) (← links)