Abca4: Gene Mutations in Japanese Patients With Stargardt Disease and Retinitis PigmentosaMARCIO AUGUSTO MORAES ALVAREZ
Quantitative Fundus Autofluorescence Distinguishes ABCA4-Associated and Non–ABCA4-Associated Bull's-Eye MaculopathyDuncker, TobiasElsevier Science2015DOI 10.1016/j.ophtha.2014.08.017
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Retinal Dystrophy Gene AtlasZahid, SarwarSpringer International Publishing Springer2018DOI 10.1007/978-3-319-10867-4|10.1007/978-3-319-10867-4_1
Evolution of ABCA4 Proteins in VertebratesAlexander N. YatsenkoSpringer2005DOI 10.1007/s00239-004-0118-4
Gene Therapy of ABCA4-Associated DiseasesAuricchio, A.Cold Spring Harbor Laboratory2015DOI 10.1101/cshperspect.a017301
Ultrawidefield Autofluoresence In Abca4 Stargardt DiseaseKlufas, Michael A.Lippincott Williams and Wilkins2018DOI 10.1097/iae.0000000000001567
Choroidal Alterations In Abca4-related RetinopathyMüller, Philipp L.Lippincott Williams and Wilkins2017DOI 10.1097/iae.0000000000001169
Macular Hyperpigmentary Changes in ABCA4-Stargardt DiseaseAbalem, Maria FernandaSpringer (Biomed Central Ltd.)2019DOI 10.1186/s40942-019-0160-4
The Lipid Translocase, ABCA4: Seeing Is BelievingNaomi Laura PollockJohn Wiley and Sons2011DOI 10.1111/j.1742-4658.2011.08169.x
Stargardt Disease: Gene Therapy Strategies for ABCA4Cristy A. KuOvid Technologies (Wolters Kluwer Health)2021DOI 10.1097/iio.0000000000000375