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Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells

dc.contributor.authorSladen, PE
dc.contributor.authorJovanovic, K
dc.contributor.authorGuarascio, R
dc.contributor.authorOttaviani, D
dc.contributor.authorSalsbury, G
dc.contributor.authorNovoselova, T
dc.contributor.authorChapple, JP
dc.contributor.authorYu-Wai-Man, P
dc.contributor.authorCheetham, ME
dc.date.accessioned2023-09-07T11:08:23Z
dc.date.available2022-05-26
dc.date.available2023-09-07T11:08:23Z
dc.date.issued2022
dc.identifier.issn0964-6906
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/90554
dc.format.extent3478 - 3493
dc.relation.ispartofHUMAN MOLECULAR GENETICS
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.titleModelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1093/hmg/ddac128
pubs.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000820591100001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue20en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume31en_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States