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

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Bibliographic Details
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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Description
ISSN:2324-9269
DOI:10.1002/mgg3.266