The hyperkinetic movement disorder of FOXG 1 ‐related epileptic–dyskinetic encephalopathy

Assessment of movement disorder in patients with FOXG1 mutations or copy number variations. FOXG1 syndrome can be defined as an epileptic–dyskinetic encephalopathy. This article is commented on by Parker on page 15 of this issue.

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Veröffentlicht in:Developmental medicine and child neurology 2016-01, Vol.58 (1), p.93-97
Hauptverfasser: Cellini, Elena, Vignoli, Aglaia, Pisano, Tiziana, Falchi, Melania, Molinaro, Anna, Accorsi, Patrizia, Bontacchio, Alessia, Pinelli, Lorenzo, Giordano, Lucio, Guerrini, Renzo
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container_end_page 97
container_issue 1
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container_title Developmental medicine and child neurology
container_volume 58
creator Cellini, Elena
Vignoli, Aglaia
Pisano, Tiziana
Falchi, Melania
Molinaro, Anna
Accorsi, Patrizia
Bontacchio, Alessia
Pinelli, Lorenzo
Giordano, Lucio
Guerrini, Renzo
description Assessment of movement disorder in patients with FOXG1 mutations or copy number variations. FOXG1 syndrome can be defined as an epileptic–dyskinetic encephalopathy. This article is commented on by Parker on page 15 of this issue.
doi_str_mv 10.1111/dmcn.12894
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title The hyperkinetic movement disorder of FOXG 1 ‐related epileptic–dyskinetic encephalopathy
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