MYBPC3 gene

Known as: FHC, MYOSIN-BINDING PROTEIN C, CARDIAC, MYBP-C 
 
National Institutes of Health

Papers overview

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2017
2017
INTRODUCTION AND OBJECTIVES Mutations in MYBPC3 are the cause of hypertrophic cardiomyopathy (HCM). Although most lead to a… (More)
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2014
2014
The etiology of hypertrophic cardiomyopathy (HCM) has been ascribed to mutations in genes encoding sarcomere proteins. In… (More)
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2014
2014
Left ventricular noncompaction (LVNC) is a clinically heterogeneous disorder characterized by a trabecular meshwork and deep… (More)
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2013
2013
Hypertrophic cardiomyopathy (HCM) is predominantly caused by mutations in genes encoding sarcomeric proteins. One of the most… (More)
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2013
2013
Myosin-binding protein C (Mybpc3)-targeted knock-in mice (KI) recapitulate typical aspects of human hypertrophic cardiomyopathy… (More)
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2009
2009
INTRODUCTION AND OBJECTIVES Mutation of a sarcomeric gene is the most frequent cause of hypertrophic cardiomyopathy. For each… (More)
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Highly Cited
2005
Highly Cited
2005
In a continuation of the conversation with Fitch, Chomsky, and Hauser on the evolution of language, we examine their defense of… (More)
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2003
2003
Mutations causing familial hypertrophic cardiomyopathy (HCM) have been described in at least 11 genes encoding cardiac sarcomeric… (More)
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2002
2002
Hypertrophic cardiomyopathy (HCM) is a genetic disorder characterized by cardiac hypertrophy caused by mutations in genes… (More)
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1996
1996
Hypercholesterolemia impairs arteriolar dilatation, but whether the vascular abnormalities accompanying this condition include… (More)
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