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A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.
Mol Vis. 2020 Nov 25;26:757-765. eCollection 2020.
Mol Vis. 2020.
PMID: 33273802
Free PMC article.
Mutation Screening of Six Exons of ABCA4 in Iranian Stargardt Disease Patients.
Darbari E, Ahmadieh H, Daftarian N, Rezaei Kanavi M, Suri F, Sabbaghi H, Elahi E.
Darbari E, et al.
J Ophthalmic Vis Res. 2022 Jan 21;17(1):51-58. doi: 10.18502/jovr.v17i1.10170. eCollection 2022 Jan-Mar.
J Ophthalmic Vis Res. 2022.
PMID: 35194496
Free PMC article.
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