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 |
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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 |
format | Article |
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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
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FOXG1
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FOXG1
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This article is commented on by Parker on page
15
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FOXG1
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FOXG1
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This article is commented on by Parker on page
15
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ispartof | Developmental medicine and child neurology, 2016-01, Vol.58 (1), p.93-97 |
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language | eng |
recordid | cdi_crossref_primary_10_1111_dmcn_12894 |
source | Wiley Free Content; Wiley Online Library All Journals |
title | The hyperkinetic movement disorder of FOXG 1 ‐related epileptic–dyskinetic encephalopathy |
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