Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency
Research output: Contribution to journal › Journal article › Research › peer-review
Original language | English |
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Journal | European Journal of Human Genetics |
Issue number | Vol. 12 |
Pages (from-to) | 673-677 |
ISSN | 1018-4813 |
Publication status | Published - 2004 |
ID: 104065