Genetic Analysis of Patients with Congenital Hereditary Endothelial Dystrophy and in vitro gene editing of SLC4A11 as a disease model

dc.contributor.guideSingh, Vivek and Muralidhar Ramappa
dc.coverage.spatialEye
dc.creator.researcherMohd Salman
dc.date.accessioned2025-11-25T12:03:43Z
dc.date.available2025-11-25T12:03:43Z
dc.date.awarded2025
dc.date.completed2025
dc.date.registered2020
dc.description.abstractAvailable newline
dc.description.notebibliography p.119-217
dc.format.accompanyingmaterialNone
dc.format.dimensions-
dc.format.extent253p.
dc.identifier.researcherid0000-0001-5200-5274
dc.identifier.urihttp://hdl.handle.net/10603/676273
dc.languageEnglish
dc.publisher.institutionL V Prasad Eye Institute
dc.publisher.placeManipal
dc.publisher.universityManipal Academy of Higher Education
dc.relation-
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordCongenital Hereditary Endothelial Dystrophy,
dc.subject.keywordCRISPR-Cas9, Knock-outs, Knock-in
dc.subject.keywordSLC4A11, Corneal dystrophies, Genome engineering,
dc.titleGenetic Analysis of Patients with Congenital Hereditary Endothelial Dystrophy and in vitro gene editing of SLC4A11 as a disease model
dc.title.alternative-
dc.type.degreePh.D.

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