A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.

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Title:	A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.
Authors:	Darbari E; School of Biology, College of Science, University of Tehran, Tehran, Iran., Zare-Abdollahi D; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Rezaei Kanavi M; Ocular Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Feizi S; Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Hosseini SB; Ocular Pathology Unit, Central Eye Bank of Iran, Tehran, Iran., Baradaran-Rafii A; Ocular Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Ahmadieh H; Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Issazadeh-Navikas S; Neuroinflammation Unit, Biotech Research and Innovation Centre (BRIC), Faculty of Health and Medical Sciences, Copenhagen Biocentre, University of Copenhagen, 2200 Copenhagen, Denmark., Elahi E; School of Biology, College of Science, University of Tehran, Tehran, Iran.
Source:	Molecular vision [Mol Vis] 2020 Nov 25; Vol. 26, pp. 757-765. Date of Electronic Publication: 2020 Nov 25 (Print Publication: 2020).
Publication Type:	Journal Article; Research Support, Non-U.S. Gov't
Journal Info:	Publisher: Molecular Vision Country of Publication: United States NLM ID: 9605351 Publication Model: eCollection Cited Medium: Internet ISSN: 1090-0535 (Electronic) Linking ISSN: 10900535 NLM ISO Abbreviation: Mol Vis Subsets: MEDLINE
Database:	MEDLINE Ultimate

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ISSN:	1090-0535