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Phenotype of PLP1-related Disorder Caused by Novel Mutation: A Case Report

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dc.contributor.authorKresojević, Nikola (26644117100)
dc.contributor.authorPetrović, Igor (7004083314)
dc.contributor.authorDobričić, Valerija (22952783800)
dc.contributor.authorTomić, Aleksandra (26654535200)
dc.contributor.authorBranković, Vesna (57192421308)
dc.contributor.authorMilić Rašić, Vedrana (6507653181)
dc.contributor.authorSvetel, Marina (6701477867)
dc.contributor.authorKostić, Vladimir (57189017751)
dc.date.accessioned2025-06-12T16:12:40Z
dc.date.available2025-06-12T16:12:40Z
dc.date.issued2018
dc.description.abstract[No abstract available]
dc.identifier.urihttps://doi.org/10.1002/mdc3.12644
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85052435229&doi=10.1002%2fmdc3.12644&partnerID=40&md5=b4026e9aecfb6add97f92d7918da9eee
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/6183
dc.subjectHereditary spastic paraplegia type 2
dc.subjectHypomyelination
dc.subjectLeukodystrophy
dc.subjectPelizaeus–Merzbacher disease
dc.subjectPLP1 gene
dc.titlePhenotype of PLP1-related Disorder Caused by Novel Mutation: A Case Report
dspace.entity.typePublication

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