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Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia.

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Title: Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia.
Authors: Toral MA; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa.; Medical Scientist Training ProgramUniversity of IowaIowa CityIowa., Velez G; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa.; Medical Scientist Training ProgramUniversity of IowaIowa CityIowa., Boudreault K; Department of OphthalmologyUniversity of MontrealMontrealQuebecCanada., Schaefer KA; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa., Xu Y; Department of OphthalmologyUniversity of MontrealMontrealQuebecCanada., Saffra N; Department of OphthalmologyMaimonides Medical CenterBrooklynNew York., Bassuk AG; Department of PediatricsUniversity of IowaIowa CityIowa., Tsang SH; The Barbara & Donald Jonas Laboratory of Regenerative Medicine and Bernard & Shirlee Brown Glaucoma LaboratoryDepartments of Ophthalmology, Pathology & Cell BiologyCollege of Physicians & SurgeonsColumbia UniversityNew York CityNew York.; Edward S. Harkness Eye InstituteNew York-Presbyterian HospitalNew York CityNew York., Mahajan VB; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa.
Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2017 Feb 26; Vol. 5 (3), pp. 202-209. Date of Electronic Publication: 2017 Feb 26 (Print Publication: 2017).
Publication Type: Journal Article
Journal Info: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: eCollection Cited Medium: Print ISSN: 2324-9269 (Print) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia.
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  Data: <searchLink fieldCode="AU" term="%22Toral+MA%22">Toral MA</searchLink>; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa.; Medical Scientist Training ProgramUniversity of IowaIowa CityIowa.<br /><searchLink fieldCode="AU" term="%22Velez+G%22">Velez G</searchLink>; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa.; Medical Scientist Training ProgramUniversity of IowaIowa CityIowa.<br /><searchLink fieldCode="AU" term="%22Boudreault+K%22">Boudreault K</searchLink>; Department of OphthalmologyUniversity of MontrealMontrealQuebecCanada.<br /><searchLink fieldCode="AU" term="%22Schaefer+KA%22">Schaefer KA</searchLink>; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa.<br /><searchLink fieldCode="AU" term="%22Xu+Y%22">Xu Y</searchLink>; Department of OphthalmologyUniversity of MontrealMontrealQuebecCanada.<br /><searchLink fieldCode="AU" term="%22Saffra+N%22">Saffra N</searchLink>; Department of OphthalmologyMaimonides Medical CenterBrooklynNew York.<br /><searchLink fieldCode="AU" term="%22Bassuk+AG%22">Bassuk AG</searchLink>; Department of PediatricsUniversity of IowaIowa CityIowa.<br /><searchLink fieldCode="AU" term="%22Tsang+SH%22">Tsang SH</searchLink>; The Barbara & Donald Jonas Laboratory of Regenerative Medicine and Bernard & Shirlee Brown Glaucoma LaboratoryDepartments of Ophthalmology, Pathology & Cell BiologyCollege of Physicians & SurgeonsColumbia UniversityNew York CityNew York.; Edward S. Harkness Eye InstituteNew York-Presbyterian HospitalNew York CityNew York.<br /><searchLink fieldCode="AU" term="%22Mahajan+VB%22">Mahajan VB</searchLink>; Omics LaboratoryUniversity of IowaIowa CityIowa.; Department of Ophthalmology and Visual SciencesUniversity of IowaIowa CityIowa.
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  Data: <searchLink fieldCode="JN" term="%22101603758%22">Molecular genetics & genomic medicine</searchLink> [Mol Genet Genomic Med] 2017 Feb 26; Vol. 5 (3), pp. 202-209. <i>Date of Electronic Publication: </i>2017 Feb 26 (<i>Print Publication: </i>2017).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22John+Wiley+%26+Sons%22">John Wiley & Sons </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101603758 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2324-9269 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2223249269%22">23249269 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Genomic Med <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.1002/mgg3.266
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              Text: 2017 Feb 26
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