Please use this identifier to cite or link to this item: http://hdl.handle.net/2067/44072
DC FieldValueLanguage
dc.contributor.authorMotta, M.en
dc.contributor.authorD'ambrosio, V.en
dc.contributor.authorVersacci, P.en
dc.contributor.authorVentriglia, F.en
dc.contributor.authorChillemi, Giovannien
dc.contributor.authorPizzuti, A.en
dc.contributor.authorTartaglia, M.en
dc.contributor.authorDe Luca, A.en
dc.contributor.authorGiancotti, A.en
dc.contributor.authorMastromoro, G.en
dc.contributor.authorChandramouli, B.en
dc.contributor.authorPinna, V.en
dc.contributor.authorPantaleoni, F.en
dc.contributor.authorDi Giosaffatte, N.en
dc.contributor.authorPetrini, S.en
dc.contributor.authorMazza, T.en
dc.date.accessioned2021-11-02T17:29:19Z-
dc.date.available2021-11-02T17:29:19Z-
dc.date.issued2019it
dc.identifier.urihttp://hdl.handle.net/2067/44072-
dc.titleClinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathyit
dc.typearticleen
dc.identifier.doi10.1002/humu.23767it
dc.relation.issn1059-7794en
dc.relation.journalHUMAN MUTATIONit
dc.relation.firstpage1046it
dc.relation.lastpage1056it
dc.relation.numberofpages10it
dc.relation.volume40it
dc.type.miur262en
local.miur.syncfalseen
item.fulltextNo Fulltext-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.journal.journalissn1098-1004-
crisitem.journal.anceE199287-
Appears in Collections:A1. Articolo in rivista
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