The variations of BOP gene in hypertrophic cardiomyopathy.
Tarih
2010Yazar
Erginel-Unaltuna, Nihan
Gulec, Çağrı
KAHVECI, Goekhan
Komurcu-Bayrak, Evrim
Bayrak, Fatih
Abaci, Neslihan
Üst veri
Tüm öğe kaydını gösterÖzet
Objective: The observation that Bop null allele mice show underdeveloped right ventricle and excessive development of left ventricle, suggests the possible relationship between human BOP gene and hypertrophic cardiomyopathy (HCMP). In our study, we investigated this possible relationship between BOP gene variations and QT dispersion, a noninvasive arrhythmic risk marker for HCMP.
Koleksiyonlar
- Makale [92796]