Neurodevelopmental disorder associated with IRF2BPL gene mutation: expanding the phenotype?

Item Type:	Letter
Title:	Neurodevelopmental disorder associated with IRF2BPL gene mutation: expanding the phenotype?
Creators Name:	Skorvanek, M. and Dusek, P. and Rydzanicz, M. and Walczak, A. and Kosinska, J. and Kostrzewa, G. and Rydzanicz, M. and Han, V. and Dosekova, P. and Gdovinova, Z. and Lehotska, Z. and Lisowski, P. and Ploski, R.
Keywords:	IRF2BPL, Brain Iron Accumulation, Epileptic Encephalopathy, Dystonia, Ataxia
Source:	Parkinsonism & Related Disorders
ISSN:	1353-8020
Publisher:	Elsevier
Volume:	62
Page Range:	239-241
Date:	24 January 2019
Official Publication:	https://doi.org/10.1016/j.parkreldis.2019.01.017
PubMed:	View item in PubMed

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