Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

    P S Andersen, DenmarkO Havndrup, DenmarkH Bundgaard, DenmarkJ C Moolman-Smook, DenmarkL A Larsen, DenmarkJ Mogensen, DenmarkP A Brink, Denmark
  • A D Børglum
  • V A Corfield, DenmarkK Kjeldsen, DenmarkJ Vuust, DenmarkM Christiansen, Denmark
  • The Department of Cardiological Medicine B
  • Department of Human Genetics
Udgivelsesdato: 2001-Dec
Original languageEnglish
JournalJournal of Medical Genetics
Issue number12
Pages (from-to)E43
Publication statusPublished - 2001

    Research areas

  • Adolescent, Adult, Aged, Cardiomyopathy, Hypertrophic, DNA Mutational Analysis, Echocardiography, Exons, Female, Gene Frequency, Humans, Male, Middle Aged, Mutation, Mutation, Missense, Myosin Light Chains, Netherlands, Pedigree, Phenotype, Polymorphism, Single-Stranded Conformational, South Africa

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ID: 18879159