Expanding the Phenotypic Spectrum of ERLIN1-Related SPG62: Report of Two Siblings With Behavioral Features and Hyperacusis

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dc.contributor.authorOzkose, Gulsah Sebnem
dc.contributor.authorTopcu, Yasemin
dc.contributor.authorAy, Beril
dc.contributor.authorOzdemir, Ozkan
dc.contributor.authorAkgun\\-Dogan, Ozlem
dc.contributor.authorNg, Ozden Hatirnaz
dc.contributor.authorAlanay, Yasemin
dc.date.accessioned2025-10-16T15:11:37Z
dc.date.issued2025
dc.identifier.doi10.1111/cge.70006
dc.identifier.otherWOS:001533296200001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/4861
dc.publisherWILEY
dc.sourceCLINICAL GENETICS
dc.subject<italic>ERLIN1<
dc.subjectitalic>
dc.subjecthereditary spastic paraplegia
dc.subjectspastic paraplegia type 62
dc.subjectultra\\-rare disorder
dc.titleExpanding the Phenotypic Spectrum of ERLIN1-Related SPG62: Report of Two Siblings With Behavioral Features and Hyperacusis
dc.typeArticle; Early Access

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