Cite
HARVARD Citation
Motta, M. et al. (2019). Clinical and functional characterization of a novel RASopathy‐causing SHOC2 mutation associated with prenatal‐onset hypertrophic cardiomyopathy. Human mutation. 40 (8), pp. 1046-1056. [Online].
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Motta, M. et al. (2019). Clinical and functional characterization of a novel RASopathy‐causing SHOC2 mutation associated with prenatal‐onset hypertrophic cardiomyopathy. Human mutation. 40 (8), pp. 1046-1056. [Online].