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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
18
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pubmed:dateCreated |
1998-4-30
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pubmed:abstractText |
Mutations in the gene for cardiac myosin-binding protein C account for approximately 15 percent of cases of familial hypertrophic cardiomyopathy. The spectrum of disease-causing mutations and the associated clinical features of these gene defects are unknown.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0028-4793
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pubmed:author |
pubmed-author:BachinskiL LLL,
pubmed-author:ChudleyA EAE,
pubmed-author:KristinssonAA,
pubmed-author:MaronB JBJ,
pubmed-author:McKennaWW,
pubmed-author:NiimuraHH,
pubmed-author:RobertiDD,
pubmed-author:SangwatanarojSS,
pubmed-author:SeidmanC ECE,
pubmed-author:SeidmanJ GJG,
pubmed-author:SollDD,
pubmed-author:WatkinsHH
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pubmed:issnType |
Print
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pubmed:day |
30
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pubmed:volume |
338
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1248-57
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:9562578-Adolescent,
pubmed-meshheading:9562578-Adult,
pubmed-meshheading:9562578-Age of Onset,
pubmed-meshheading:9562578-Aged,
pubmed-meshheading:9562578-Aged, 80 and over,
pubmed-meshheading:9562578-Cardiomyopathy, Hypertrophic,
pubmed-meshheading:9562578-Carrier Proteins,
pubmed-meshheading:9562578-Child,
pubmed-meshheading:9562578-DNA Mutational Analysis,
pubmed-meshheading:9562578-Female,
pubmed-meshheading:9562578-Genotype,
pubmed-meshheading:9562578-Humans,
pubmed-meshheading:9562578-Male,
pubmed-meshheading:9562578-Middle Aged,
pubmed-meshheading:9562578-Mutation,
pubmed-meshheading:9562578-Myosins,
pubmed-meshheading:9562578-Pedigree,
pubmed-meshheading:9562578-Penetrance,
pubmed-meshheading:9562578-Survival Analysis
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pubmed:year |
1998
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pubmed:articleTitle |
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
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pubmed:affiliation |
Howard Hughes Medical Institute, Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Multicenter Study
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