Episodic movement disorders: from phenotype to genotype and back.
about
PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects.Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.Aberrant Sensory Gating of the Primary Somatosensory Cortex Contributes to the Motor Circuit Dysfunction in Paroxysmal Kinesigenic Dyskinesia
P2860
Episodic movement disorders: from phenotype to genotype and back.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Episodic movement disorders: from phenotype to genotype and back.
@en
type
label
Episodic movement disorders: from phenotype to genotype and back.
@en
prefLabel
Episodic movement disorders: from phenotype to genotype and back.
@en
P2860
P1476
Episodic movement disorders: from phenotype to genotype and back.
@en
P2093
Knut Brockmann
P2860
P2888
P356
10.1007/S11910-013-0379-7
P577
2013-10-01T00:00:00Z
P6179
1014843652