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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
1995-7-31
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pubmed:abstractText |
Hypertrophic cardiomyopathy (HCM) is characterized by myocardial hypertrophy of unknown etiology. Missense mutations of the cardiac beta-myosin-heavy-chain (beta-MHC) gene that may be responsible for cardiac hypertrophy have been detected in patients with HCM. On the other hand, gross structural abnormalities in the cardiac beta-MHC gene, ie, an alpha/beta hybrid gene and partial deletion of the gene, have also been reported. The direct correlation between gross abnormalities and development of HCM is not well understood.
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pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
|
pubmed:issn |
0009-7322
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
91
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
N
|
pubmed:pagination |
2911-5
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:7796500-Base Sequence,
pubmed-meshheading:7796500-Cardiomyopathy, Hypertrophic,
pubmed-meshheading:7796500-Humans,
pubmed-meshheading:7796500-Molecular Sequence Data,
pubmed-meshheading:7796500-Mutation,
pubmed-meshheading:7796500-Myosins,
pubmed-meshheading:7796500-Polymerase Chain Reaction,
pubmed-meshheading:7796500-Polymorphism, Genetic
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pubmed:year |
1995
|
pubmed:articleTitle |
A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy.
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pubmed:affiliation |
Third Department of Internal Medicine, Kurume University School of Medicine, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|