Please use this identifier to cite or link to this item: http://hdl.handle.net/2067/44072
Title: Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy
Authors: Motta, M.
D'ambrosio, V.
Versacci, P.
Ventriglia, F.
Chillemi, Giovanni 
Pizzuti, A.
Tartaglia, M.
De Luca, A.
Giancotti, A.
Mastromoro, G.
Chandramouli, B.
Pinna, V.
Pantaleoni, F.
Di Giosaffatte, N.
Petrini, S.
Mazza, T.
Journal: HUMAN MUTATION 
Issue Date: 2019
URI: http://hdl.handle.net/2067/44072
DOI: 10.1002/humu.23767
Appears in Collections:A1. Articolo in rivista

Show full item record

Page view(s)

56
Last Week
0
Last month
0
checked on Feb 28, 2024

Google ScholarTM

Check

Altmetric


All documents in the "Unitus Open Access" community are published as open access.
All documents in the community "Prodotti della Ricerca" are restricted access unless otherwise indicated for specific documents