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Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review

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dc.contributor.authorÇomu, Sinan
dc.contributor.authorSinan Çomu
dc.contributor.authorMesut Güngör
dc.contributor.authorYonca Anık
dc.contributor.authorBülent Kara
dc.contributor.orcid0000-0002-9385-3787
dc.contributor.orcid0000-0003-1594-0006
dc.contributor.orcid0000-0002-6768-2574
dc.contributor.orcid0000-0003-3780-6596
dc.date.accessioned2025-11-13T12:04:09Z
dc.date.issued2021-11-09
dc.identifier.doihttps://doi.org/10.1055/s-0041-1739387
dc.identifier.endpage122
dc.identifier.issn2146-4596
dc.identifier.issue02
dc.identifier.openalexW3214675345
dc.identifier.startpage116
dc.identifier.urihttps://hdl.handle.net/11421/8858
dc.identifier.urihttps://doi.org/10.1055/s-0041-1739387
dc.identifier.volume13
dc.language.isoen
dc.relation.ispartofJournal of Pediatric Genetics
dc.rightsopenAccess
dc.subjectDecussation
dc.subjectMedicine
dc.subjectScoliosis
dc.subjectCompound heterozygosity
dc.subjectBrainstem
dc.subjectMedial longitudinal fasciculus
dc.subjectAnatomy
dc.subjectMutation
dc.subjectSurgery
dc.subjectMidbrain
dc.subjectInternal medicine
dc.subjectGenetics
dc.subjectBiology
dc.subject.sdg3
dc.titleCompound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review
dc.typeArticle
dspace.entity.typePublication
local.authorid.openalexA5047661961

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