Deep Myocardial Phenotyping of the Noonan Syndrome-causing Mutation RIT1<sup>F82L/+</sup> In Vitro and RAS/MAPK Signalling as a Therapeutic Target
Cited by 0
Related Papers
The <scp>8th International RASopathies Symposium</scp>: Expanding research and care practice through global collaboration and advocacy
|American Journal of Medical Genetics Part A|2023|7