Phenotypic variability in a dystonia family with mutations in the manganese transporter gene

CCS Delnooz; RA Wevers; Marialuisa Quadri; PT Clayton; PB Mills; K Tuschl; EJ Steenbergen; Vincenzo Bonifati; BPC van de Warrenburg

doi:10.1002/mds.25390

Phenotypic variability in a dystonia family with mutations in the manganese transporter gene

CCS Delnooz, RA Wevers, Marialuisa Quadri, PT Clayton, PB Mills, K Tuschl, EJ Steenbergen, Vincenzo Bonifati, BPC van de Warrenburg

Clinical Genetics

Research output: Contribution to journal › Article › Academic › peer-review

9 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	685-686
Number of pages	2
Journal	Movement Disorders
Volume	28
Issue number	5
DOIs	https://doi.org/10.1002/mds.25390
Publication status	Published - 2013

Research programs

EMC MGC-02-96-01

Access to Document

10.1002/mds.25390

http://hdl.handle.net/1765/53935

Cite this

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title = "Phenotypic variability in a dystonia family with mutations in the manganese transporter gene",

author = "CCS Delnooz and RA Wevers and Marialuisa Quadri and PT Clayton and PB Mills and K Tuschl and EJ Steenbergen and Vincenzo Bonifati and {van de Warrenburg}, BPC",

year = "2013",

doi = "10.1002/mds.25390",

language = "Undefined/Unknown",

volume = "28",

pages = "685--686",

journal = "Movement Disorders",

issn = "0885-3185",

publisher = "John Wiley & Sons Inc.",

number = "5",

}

TY - JOUR

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AU - Delnooz, CCS

AU - Wevers, RA

AU - Quadri, Marialuisa

AU - Clayton, PT

AU - Mills, PB

AU - Tuschl, K

AU - Steenbergen, EJ

AU - Bonifati, Vincenzo

AU - van de Warrenburg, BPC

PY - 2013

Y1 - 2013

U2 - 10.1002/mds.25390

DO - 10.1002/mds.25390

M3 - Article

C2 - 23592301

SN - 0885-3185

VL - 28

SP - 685

EP - 686

JO - Movement Disorders

JF - Movement Disorders

IS - 5

ER -