normal phenotype
• despite most causative mutations in TNNT2 resulting in cardiomyopathy in humans being dominant, heterozygous mice are viable with normal heart structure and function
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
NOT | dilated cardiomyopathy 1D | DOID:0110426 |
OMIM:601494 |
J:141967 |