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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

Semantic Scholar uses AI to extract papers important to this topic.
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
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
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
Review
2013
Review
2013
Left ventricular noncompaction (LVNC) is a relatively common genetic cardiomyopathy, characterized by prominent trabeculations… Expand
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