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

Date

2018

Authors

Kresojević, Nikola (26644117100)

Petrović, Igor (7004083314)

Dobričić, Valerija (22952783800)

Tomić, Aleksandra (26654535200)

Branković, Vesna (57192421308)

Milić Rašić, Vedrana (6507653181)

Svetel, Marina (6701477867)

Kostić, Vladimir (57189017751)

Abstract

[No abstract available]

Keywords

Hereditary spastic paraplegia type 2, Hypomyelination, Leukodystrophy, Pelizaeus–Merzbacher disease, PLP1 gene

URI

https://doi.org/10.1002/mdc3.12644
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052435229&doi=10.1002%2fmdc3.12644&partnerID=40&md5=b4026e9aecfb6add97f92d7918da9eee
https://remedy.med.bg.ac.rs/handle/123456789/12895

Collections

Publikacije / Publications