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

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Bibliographic Details
Published in:	Movement disorders clinical practice (Hoboken, N.J.) N.J.), 2018-09, Vol.5 (5), p.548-550
Main Authors:	Kresojević, Nikola, Petrović, Igor, Dobričić, Valerija, Tomić, Aleksandra, Branković, Vesna, Milić Rašić, Vedrana, Svetel, Marina, Kostić, Vladimir
Format:	Article
Language:	English
Subjects:	Case Report Case Reports Hereditary spastic paraplegia type 2 Hypomyelination Leukodystrophy Pelizaeus–Merzbacher disease PLP1 gene Spasticity
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Online Access:	Get full text
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