Pollock, Naomi L.Callaghan, Richard2015-12-071742-464Xhttp://hdl.handle.net/1885/25060Mutations 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 numberKeywords: 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 disease201110.1111/j.1742-4658.2011.08169.x2016-02-24