Cite
MLA Citation
Marialetizia Motta et al.. “Clinical and functional characterization of a novel RASopathy‐causing SHOC2 mutation associated with prenatal‐onset hypertrophic cardiomyopathy.” Human mutation, vol. 40, no. 8, 2019, pp. 1046–1056. http://access.bl.uk/ark:/81055/vdc_100089551947.0x000030