Identification of a novel Ala797Thr mutation in exon 21 of the β-myosin heavy chain gene in hypertrophic cardiomyopathy

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dc.contributor.authorMoolman J.C.
dc.contributor.authorBrink P.A.
dc.contributor.authorCorfield V.A.
dc.date.accessioned2011-05-15T16:16:33Z
dc.date.available2011-05-15T16:16:33Z
dc.date.issued1995
dc.description.abstract[No abstract available]
dc.description.versionArticle
dc.identifier.citationHuman Mutation
dc.identifier.citation6
dc.identifier.citation2
dc.identifier.issn10597794
dc.identifier.other10.1002/humu.1380060219
dc.identifier.urihttp://hdl.handle.net/10019.1/13830
dc.subjectalanine
dc.subjectmyosin heavy chain
dc.subjectthreonine
dc.subjectarticle
dc.subjectclinical article
dc.subjectexon
dc.subjectgene mutation
dc.subjecthuman
dc.subjecthuman cell
dc.subjecthypertrophic cardiomyopathy
dc.subjectpolymerase chain reaction
dc.subjectpriority journal
dc.subjectBase Sequence
dc.subjectCardiomyopathy, Hypertrophic
dc.subjectDNA Mutational Analysis
dc.subjectExons
dc.subjectHuman
dc.subjectMolecular Sequence Data
dc.subjectMutation
dc.subjectMyosin Heavy Chains
dc.subjectPolymerase Chain Reaction
dc.subjectPolymorphism, Single-Stranded Conformational
dc.subjectSouth Africa
dc.titleIdentification of a novel Ala797Thr mutation in exon 21 of the β-myosin heavy chain gene in hypertrophic cardiomyopathy
dc.typeArticle
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