Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia

Kailash P. Bhatia; Susanne A. Schneider

doi:10.1002/mds.25038

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia

Kailash P. Bhatia^*, Susanne A. Schneider

^*Corresponding author for this work

Department of Neurology

University of London

11 Citations (Scopus)

Original language	English
Journal	Movement Disorders
Volume	27
Issue number	6
Number of pages	1
ISSN	0885-3185
DOIs	https://doi.org/10.1002/mds.25038
Publication status	Published - 01.05.2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being
SDG 10 Reduced Inequalities

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title = "Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia",

author = "Bhatia, \{Kailash P.\} and Schneider, \{Susanne A.\}",

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T1 - Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia

AU - Bhatia, Kailash P.

AU - Schneider, Susanne A.

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DO - 10.1002/mds.25038

M3 - Comments/Debates

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SN - 0885-3185

VL - 27

JO - Movement Disorders

JF - Movement Disorders

IS - 6

ER -

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia

UN SDGs

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