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

P. S. Andersen*, O. Havndrup, H. Bundgaard, J. C. Moolman-Smook, L. A. Larsen, J. Mogensen, P. A. Brink, A. D. Børglum, V. A. Corfield, K. Kjeldsen, J. Vuust, M. Christiansen

*Corresponding author for this work

    Research output: Contribution to journalLetterResearchpeer-review

    Original languageEnglish
    Pages (from-to)E43
    JournalJournal of medical genetics
    Volume38
    Issue number12
    Publication statusPublished - 1 Dec 2001

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