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. |
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| 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 |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 33273802 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family. – Name: Author Label: Authors Group: Au 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. – Name: TitleSource Label: Source Group: Src 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). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src 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 |
| RecordInfo | BibRecord: BibEntity: Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 757 Titles: – TitleFull: A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Darbari E – PersonEntity: Name: NameFull: Zare-Abdollahi D – PersonEntity: Name: NameFull: Alavi A – PersonEntity: Name: NameFull: Rezaei Kanavi M – PersonEntity: Name: NameFull: Feizi S – PersonEntity: Name: NameFull: Hosseini SB – PersonEntity: Name: NameFull: Baradaran-Rafii A – PersonEntity: Name: NameFull: Ahmadieh H – PersonEntity: Name: NameFull: Issazadeh-Navikas S – PersonEntity: Name: NameFull: Elahi E IsPartOfRelationships: – BibEntity: Dates: – D: 25 M: 11 Text: 2020 Nov 25 Type: published Y: 2020 Identifiers: – Type: issn-electronic Value: 1090-0535 Numbering: – Type: volume Value: 26 Titles: – TitleFull: Molecular vision Type: main |
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