Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

P.S. Andersen; O. Havndrup; H. Bundgaard; Lars Allan Larsen; J. Vuust; A.K. Pedersen; K. Kjeldsen; M. Christiansen

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

P.S. Andersen, O. Havndrup, H. Bundgaard, Lars Allan Larsen, J. Vuust, A.K. Pedersen, K. Kjeldsen, M. Christiansen

49 Citations (Scopus)

Original language	English
Journal	European Journal of Human Genetics
Issue number	Vol. 12
Pages (from-to)	673-677
ISSN	1018-4813
Publication status	Published - 2004

Cite this

Andersen, P. S., Havndrup, O., Bundgaard, H., Larsen, L. A., Vuust, J., Pedersen, A. K., Kjeldsen, K., & Christiansen, M. (2004). Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency. European Journal of Human Genetics, (Vol. 12), 673-677.

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency. / Andersen, P.S.; Havndrup, O.; Bundgaard, H. et al.
In: European Journal of Human Genetics, No. Vol. 12, 2004, p. 673-677.

Research output: Contribution to journal › Journal article › Research › peer-review

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AU - Bundgaard, H.

AU - Larsen, Lars Allan

AU - Vuust, J.

AU - Pedersen, A.K.

AU - Kjeldsen, K.

AU - Christiansen, M.

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