Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy

Author(s)
Motta, M.
D'ambrosio, V.
Versacci, P.
Ventriglia, F.
Date Issued
2019
Type
article
Volume
40
Start Page
1046
End Page
1056
DOI
ISSN
1059-7794
Journal
Handle