Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy

Tarih
2001
Yazar
Fleck, E
Regitz-Zagrosek, V
Wollnik, B
Frantz, E
Hetzer, R
Erdmann, J
Raible, J
Maki-Abadi, J
Hummel, M
Hammann, J
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Özet
Objectives We studied the clinical and genetic features of hypertrophic cardiomyopathy (HCM) caused by mutations in the myosin-binding protein C gene (MYBPC3) in 110 consecutive, unrelated patients and family members of European descent.
Bağlantı
http://hdl.handle.net/20.500.12627/34370
https://doi.org/10.1016/s0735-1097(01)01387-0
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