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MYH7 gene

Known as: MYOSIN, CARDIAC, HEAVY CHAIN, BETA, MYOSIN, HEAVY CHAIN 7, CARDIAC MUSCLE, BETA, CMD1S 
 
National Institutes of Health

Papers overview

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2017
2017
Familial dilated cardiomyopathy (DCM) is characterized by ventricular dilation and depressed myocardial performance. It is a… Expand
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2016
2016
TIA1 mutations cause Welander distal myopathy. MYH7 mutations result in various clinical phenotypes, including Laing distal… Expand
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2016
2016
Here we report on a case of MYH7-related myopathy in a boy with early onset of muscular weakness and delayed motor development in… Expand
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2016
2016
BackgroundMyosin heavy chain 7 related myopathies are rare disorders characterized by a wide phenotypic spectrum and… Expand
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2016
2016
To search for genes associated with migratory phenotypes in songbirds, we selected candidate genes through annotations from the… Expand
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2015
2015
Mutations in the beta-myosin heavy chain gene (MYH7) cause different muscle disorders. The specific molecular pathobiological… Expand
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Highly Cited
2014
Highly Cited
2014
Laing early onset distal myopathy and myosin storage myopathy are caused by mutations of slow skeletal/β‐cardiac myosin heavy… Expand
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Highly Cited
2009
Highly Cited
2009
INTRODUCTION AND OBJECTIVES Mutation of a sarcomeric gene is the most frequent cause of hypertrophic cardiomyopathy. For each… Expand
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2001
2001
An unusual clinical history of a 23-year-old male proband with obstructive hypertrophic cardiomyopathy associated with a rare… Expand
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