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A novel causative functional mutation in GATA6 gene is responsible for familial dilated cardiomyopathy as supported by in silico functional analysis

dc.contributor.authorKhazamipour, Afrouz
dc.contributor.authorGholampour-Faroji, Nazanin
dc.contributor.authorZeraati, Tina
dc.contributor.authorVakilian, Farveh
dc.contributor.authorHaddad-Mashadrizeh, Aliakbar
dc.contributor.authorGhayour Mobarhan, Majid
dc.contributor.authorPasdar, Alireza
dc.contributor.institutionUniversity of Aberdeen.Applied Medicineen
dc.date.accessioned2023-09-04T07:41:06Z
dc.date.available2023-09-04T07:41:06Z
dc.date.issued2022-12
dc.descriptionFunding Information: This study was supported by grants from the Mashhad University of Medical Sciences (Grant Number 980955). The authors thank the management of advanced computational centre, Khayyam Innovation Ecosystem, Mashhad, Iran for providing the facilities and encouragement to carry out this research work.en
dc.description.statusPeer revieweden
dc.format.extent13
dc.format.extent1493130
dc.identifier260145189
dc.identifier95f8f6ba-710f-4c82-944a-d817b71806a0
dc.identifier85135819277
dc.identifier35962153
dc.identifier.citationKhazamipour, A, Gholampour-Faroji, N, Zeraati, T, Vakilian, F, Haddad-Mashadrizeh, A, Ghayour Mobarhan, M & Pasdar, A 2022, 'A novel causative functional mutation in GATA6 gene is responsible for familial dilated cardiomyopathy as supported by in silico functional analysis', Scientific Reports, vol. 12, 13752. https://doi.org/10.1038/s41598-022-13993-6en
dc.identifier.doi10.1038/s41598-022-13993-6
dc.identifier.issn2045-2322
dc.identifier.otherORCID: /0000-0002-7864-9729/work/141718614
dc.identifier.urihttps://hdl.handle.net/2164/21611
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85135819277&partnerID=8YFLogxKen
dc.identifier.vol12en
dc.language.isoeng
dc.relation.ispartofScientific Reportsen
dc.subjectRC Internal medicineen
dc.subjectQH426 Geneticsen
dc.subjectGeneralen
dc.subjectSupplementary Dataen
dc.subject.lccRCen
dc.subject.lccQH426en
dc.titleA novel causative functional mutation in GATA6 gene is responsible for familial dilated cardiomyopathy as supported by in silico functional analysisen
dc.typeJournal articleen

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