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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 report
Radovan Haluza, Štěpánka Halouzková, Martin Bunček
Experimental and clinical cardiology.
2001 ;
Roč. 6 (č. 4) :
s. 223-227.
Language English Country Canada
Document type Case Reports
Persistent link
https://www.medvik.cz/link/bmc03006621
Online
NLK
Free Medical Journals
from Spring 2001 to Spring 2013
PubMed Central
from 2001 to 2013
Europe PubMed Central
from 2001 to 2013
- MeSH
- Gene Amplification MeSH
- Adult MeSH
- Exons MeSH
- Cardiomyopathy, Hypertrophic genetics pathology MeSH
- Humans MeSH
- Mutation MeSH
- Cardiac Myosins genetics MeSH
- Myosin Heavy Chains genetics MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Case Reports MeSH
Bibliography, etc.
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