Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain

Keyphrases

• Familial Hypertrophic Cardiomyopathy 100%
• Novel mutation 100%
• Exon 7 100%
• Myosin Heavy Chain (MyHC) 100%
• ATP Binding 100%
• Binding Region 100%
• MYH7 Gene 100%
• Myocardial Hypertrophy 100%
• Hypertrophic Cardiomyopathy 50%
• Sarcomere Proteins 50%
• ATP Hydrolysis 50%
• Three-generation 50%
• Cardiac Sarcomere 50%
• Cardiac Myosin Heavy Chain 50%
• Myosin Head 50%
• Autosomal Dominant Disorder 50%
• Threonine 50%
• P-loop 50%
• MYH7 50%
• Mechanical Energy 50%
• Phosphate Binding 50%
• Gene Encoding 50%
• Myosin Heavy Chain Gene 50%
• Arginine Residues 50%
• F-helix 50%

Biochemistry, Genetics and Molecular Biology

• Missense Mutation 100%
• Adenosine Triphosphate 100%
• MYH7 100%
• Heavy Meromyosin 100%
• Exon 66%
• Autosomal Dominant Inheritance 33%
• Enzymatic Hydrolysis 33%
• Myosin Head 33%
• Arginine 33%
• F Helix 33%
• Threonine 33%