Louw et al., 2018
- Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.
PLoS Genetics
14:e1007138
Full text @ PLoS Genet.
Marker Type | Symbol | Name |
---|---|---|
Gene | kif20a | kinesin family member 20A |
Gene | tp53 | tumor protein p53 |