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The lipid translocase, ABCA4: seeing is believing

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dc.contributor.authorPollock, Naomi L.
dc.contributor.authorCallaghan, Richard
dc.date.accessioned2015-12-07T22:44:06Z
dc.date.issued2011
dc.date.updated2016-02-24T10:26:19Z
dc.description.abstractMutations to members of the A subfamily of ATP binding cassette (ABC) proteins are responsible for a number of diseases; typically they are associated with aberrant cellular lipid transport processes. Mutations to the ABCA4 protein are linked to a number
dc.identifier.issn1742-464X
dc.identifier.urihttp://hdl.handle.net/1885/25060
dc.publisherBlackwell Publishing Ltd
dc.sourceThe FEBS Journal
dc.subjectKeywords: ABC transporter; ABC transporter a4; phosphatidylethanolamine; retinal; unclassified drug; gene mutation; genotype; human; lipid transport; nonhuman; phenotype; priority journal; protein function; retinitis pigmentosa; review; Stargardt disease; visual di ABC transporter; all-trans-retinal; phospholipid translocase; Stargardt disease
dc.titleThe lipid translocase, ABCA4: seeing is believing
dc.typeJournal article
local.bibliographicCitation.issue18
local.bibliographicCitation.lastpage3214
local.bibliographicCitation.startpage3204
local.contributor.affiliationPollock, Naomi L., University of Oxford
local.contributor.affiliationCallaghan, Richard, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidCallaghan, Richard, u5103268
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor060199 - Biochemistry and Cell Biology not elsewhere classified
local.identifier.absfor060112 - Structural Biology (incl. Macromolecular Modelling)
local.identifier.absfor060110 - Receptors and Membrane Biology
local.identifier.absseo970106 - Expanding Knowledge in the Biological Sciences
local.identifier.ariespublicationu4008405xPUB36
local.identifier.citationvolume278
local.identifier.doi10.1111/j.1742-4658.2011.08169.x
local.identifier.scopusID2-s2.0-80052509365
local.type.statusPublished Version

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