Skip to search formSkip to main contentSkip to account menu

MYH7 gene

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

Related topics

Related topics

2 relations
CARDIOMYOPATHY, DILATED, 1EMYH6 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
2016
2016
Distal myopathy with coexisting heterozygous TIA1 and MYH7 Variants
2016
2016
Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features – a case report
BackgroundMyosin heavy chain 7 related myopathies are rare disorders characterized by a wide phenotypic spectrum and… 
2016
2016
Exploring novel candidate genes from the Mouse Genome Informatics database: Potential implications for avian migration research.
To search for genes associated with migratory phenotypes in songbirds, we selected candidate genes through annotations from the… 
2016
2016
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion
2015
2015
A rare mutation in MYH7 gene occurs with overlapping phenotype.
Highly Cited
2014
Highly Cited
2014
Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β‐Cardiac Myosin (MYH7) Distal Myopathy
Laing early onset distal myopathy and myosin storage myopathy are caused by mutations of slow skeletal/β‐cardiac myosin heavy… 
Review
2013
Review
2013
Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7
Left ventricular noncompaction (LVNC) is a relatively common genetic cardiomyopathy, characterized by prominent trabeculations… 
Highly Cited
2009
Highly Cited
2009
[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].
2001
2001
Familial hypertrophic cardiomyopathy owing to double heterozygosity for a 403Arg--> Trp mutation in exon 13 of the MYH7 gene and a novel mutation, 453Arg--> His, in exon 14 of the MYH7 gene: A case…
An unusual clinical history of a 23-year-old male proband with obstructive hypertrophic cardiomyopathy associated with a rare… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)