The genetic basis of hypertrophic cardiomyopathy in cats and humans.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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2015年學術文章

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The genetic basis of hypertrophic cardiomyopathy in cats and humans.

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The genetic basis of hypertrophic cardiomyopathy in cats and humans.

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The genetic basis of hypertrophic cardiomyopathy in cats and humans.

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P1476

The genetic basis of hypertrophic cardiomyopathy in cats and humans

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P2093

Mark D Kittleson

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Samantha P Harris

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P2860

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

Human cardiac myosin heavy chain genes and their linkage in the genome

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

Structure, stability and dynamics of the central domain of cardiac myosin binding protein C (MyBP-C): implications for multidomain assembly and causes for cardiomyopathy

Myosin Binding Protein C Positioned to Play a Key Role in Regulation of Muscle Contraction: Structure and Interactions of Domain C1

The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product

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S53-73

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scholarly article

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10.1016/J.JVC.2015.03.001

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17 Suppl 1

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K M Meurs

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2015-12-01T00:00:00Z

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290624850

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26776594

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