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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  Data: A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.
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  Data: <searchLink fieldCode="AU" term="%22Darbari+E%22">Darbari E</searchLink>; School of Biology, College of Science, University of Tehran, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Zare-Abdollahi+D%22">Zare-Abdollahi D</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Alavi+A%22">Alavi A</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Rezaei+Kanavi+M%22">Rezaei Kanavi M</searchLink>; Ocular Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Feizi+S%22">Feizi S</searchLink>; Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Hosseini+SB%22">Hosseini SB</searchLink>; Ocular Pathology Unit, Central Eye Bank of Iran, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Baradaran-Rafii+A%22">Baradaran-Rafii A</searchLink>; Ocular Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Ahmadieh+H%22">Ahmadieh H</searchLink>; Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Issazadeh-Navikas+S%22">Issazadeh-Navikas S</searchLink>; Neuroinflammation Unit, Biotech Research and Innovation Centre (BRIC), Faculty of Health and Medical Sciences, Copenhagen Biocentre, University of Copenhagen, 2200 Copenhagen, Denmark.<br /><searchLink fieldCode="AU" term="%22Elahi+E%22">Elahi E</searchLink>; School of Biology, College of Science, University of Tehran, Tehran, Iran.
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  Data: <searchLink fieldCode="JN" term="%229605351%22">Molecular vision</searchLink> [Mol Vis] 2020 Nov 25; Vol. 26, pp. 757-765. <i>Date of Electronic Publication: </i>2020 Nov 25 (<i>Print Publication: </i>2020).
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  Data: Journal Article; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Molecular+Vision%22">Molecular Vision </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9605351 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1090-0535 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210900535%22">10900535 </searchLink><i>NLM ISO Abbreviation: </i>Mol Vis <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=33273802
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      – TitleFull: A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.
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              Text: 2020 Nov 25
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