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

Erdmann, J; Raible, J; Maki-Abadi, J; Hummel, M; Hammann, J; Wollnik, B; Frantz, E; Fleck, E; Hetzer, R; Regitz-Zagrosek, V

doi:10.1016/s0735-1097(01)01387-0

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

Atıf İçin Kopyala

Erdmann J., Raible J., Maki-Abadi J., Hummel M., Hammann J., Wollnik B., ...Daha Fazla

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, cilt.38, sa.2, ss.322-330, 2001 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 38 Sayı: 2
Basım Tarihi: 2001
Doi Numarası: 10.1016/s0735-1097(01)01387-0
Dergi Adı: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.322-330
İstanbul Üniversitesi Adresli: Hayır

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.