cardiac Troponin T peptide (ab47005)
- Cardiac muscle troponin TCardiomyopathy dilated 1D (autosomal dominant)Cardiomyopathy hypertrophic 2
- CMD1DCMH2CMPD2cTnTLVNC6MGC3889OTTHUMP00000033864OTTHUMP00000033865OTTHUMP00000033866OTTHUMP00000033867OTTHUMP00000033870OTTHUMP00000218095RCM3TNNT 2TNNT2TNNT2_HUMANTnTCTroponin T cardiac muscleTroponin T type 2 (cardiac)Troponin T type 2 cardiacTroponin T, cardiac muscleTroponin T2Troponin T2 cardiac
Defects in TNNT2 are the cause of cardiomyopathy dilated type 1D (CMD1D) [MIM:601494]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.
Defects in TNNT2 are the cause of cardiomyopathy familial restrictive type 3 (RCM3) [MIM:612422]. Restrictive cardiomyopathy is a heart disorder characterized by impaired filling of the ventricles with reduced diastolic volume, in the presence of normal or near normal wall thickness and systolic function.
References for cardiac Troponin T peptide (ab47005)
ab47005 has not yet been referenced specifically in any publications.