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Clinical and functional characterization of a novel RASopathy‐causing SHOC2 mutation associated with prenatal‐onset hypertrophic cardiomyopathy
Motta, Marialetizia, Giancotti, Antonella, Mastromoro, Gioia, Chandramouli, Balasubramanian, Pinna, Valentina, Pantaleoni, Francesca, Di Giosaffatte, Niccolò, Petrini, Stefania, Mazza, Tommaso, D’AmbrLanguage:
english
Journal:
Human Mutation
DOI:
10.1002/humu.23767
Date:
May, 2019
File:
PDF, 1.95 MB
english, 2019