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ERLIN1-Related Hereditary Spastic Paraplegia (SPG62): A Recurrent Variant Expanding Phenotype

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dc.contributor.authorOzkose-Iyigel, Gulsah Sebnem
dc.contributor.authorTopcu, Yasemin
dc.contributor.authorAy, Beril
dc.contributor.authorOzdemir, Ozkan
dc.contributor.authorDogan, Ozlem Akgun
dc.contributor.authorNg, Ozden Hatirnaz
dc.contributor.authorAlanay, Yasemin
dc.date.accessioned2026-11-05T11:02:08Z
dc.date.issued2025
dc.description.pages327-327
dc.description.volume33
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10864
dc.identifier.wosWOS:001688659402012
dc.language.isoen
dc.publisherSPRINGERNATURE
dc.relation.conference58th Conference of the European-Society-of-Human-Genetics (ESHG)
dc.relation.ispartofEUROPEAN JOURNAL OF HUMAN GENETICS
dc.subjectBiochemistry & Molecular Biology
dc.subjectGenetics & Heredity
dc.titleERLIN1-Related Hereditary Spastic Paraplegia (SPG62): A Recurrent Variant Expanding Phenotype
dc.typeMeeting Abstract
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.editionConference Proceedings Citation Index - Science (CPCI-S)
oaire.citation.endPage327
oaire.citation.startPage327
oaire.citation.volume33
person.identifier.ridA-1516-2016
person.identifier.ridW-8018-2018
person.identifier.ridAAI-9947-2021

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