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

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Item Type:	Letter
Title:	Neurodevelopmental disorder associated with IRF2BPL gene mutation: expanding the phenotype?
Creators:	Skorvanek, M., Dusek, P. ORCID: https://orcid.org/0000-0003-4877-9642, Rydzanicz, M., Walczak, A., Kosinska, J., Kostrzewa, G., Rydzanicz, M., Han, V., Dosekova, P., Gdovinova, Z., Lehotska, Z., Lisowski, P. ORCID: https://orcid.org/0000-0002-3634-1072 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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