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Hypertrophic cardiomyopathy: how do mutations lead to disease?

Hypertrophic cardiomyopathy: how do mutations lead to disease?

http://www.wikidata.org/entity/Q38203157

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Myocardial fibrosis: biomedical research from bench to bedside.Sex-related differences in the associations between plasma free fatty acid levels and clinical features in patients with hypertrophic cardiomyopathy.Contextualizing Genetics for Regional Heart Failure Care Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.A Cardiomyopathy Mutation in the Myosin Essential Light Chain Alters Actomyosin Structure.Successful knock-in of Hypertrophic Cardiomyopathy-mutation R723G into the MYH7 gene mimics HCM pathology in pigs.Actin-Myosin Interaction: Structure, Function and Drug Discovery

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Hypertrophic cardiomyopathy: how do mutations lead to disease?

http://www.wikidata.org/entity/Q38203157

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Hypertrophic cardiomyopathy: how do mutations lead to disease?

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Hypertrophic cardiomyopathy: how do mutations lead to disease?

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Hypertrophic cardiomyopathy: how do mutations lead to disease?

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Arquivos Brasileiros De Cardiologia

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Hypertrophic cardiomyopathy: how do mutations lead to disease?

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Alexandre Costa Pereira

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Júlia Daher Carneiro Marsiglia

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Creative Commons Attribution-NonCommercial 3.0 Unported

P2860

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene.

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy

Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy

Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

Zebrafish in the study of early cardiac development

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency

Regulation of the interaction between actin and myosin subfragment 1: evidence for three states of the thin filament

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295-304

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scholarly article

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10.5935/ABC.20140022

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3

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2014-03-01T00:00:00Z

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24714796

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hypertrophic cardiomyopathy

genetic variation

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3987320

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