The phenotypic spectrum of DYT24 due to ANO3 mutations-Reference-Cited by-同舟云学术

The phenotypic spectrum of DYT24 due to ANO3 mutations

Published:2014-01-17 Issue:7 Volume:29 Page:928-934
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Stamelou Maria¹²,Charlesworth Gavin³,Cordivari Carla⁴,Schneider Susanne A.¹⁵,Kägi Georg¹⁶,Sheerin Una-Marie³,Rubio-Agusti Ignacio¹,Batla Amit¹,Houlden Henry³,Wood Nicholas W.³,Bhatia Kailash P.¹

Affiliation:

1. Sobell Department of Motor Neuroscience and Movement Disorders; University College London (UCL) Institute of Neurology; London United Kingdom

2. Neurology Clinic; Attiko Hospital, University of Athens; Greece

3. Department of Molecular Neuroscience; UCL Institute of Neurology; London United Kingdom

4. Department of Clinical Neurophysiology; National Hospital for Neurology and Neurosurgery; London United Kingdom

5. Department of Neurology; University of Kiel; Kiel Germany

6. Department of Neurology; Kantonsspital St. Gallen St. Gallen Switzerland

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference24 articles.

1. Mutations in ANO3 cause cranio-cervical dystonia: a novel molecular mechanism;Charlesworth;Am J Hum Genet,2012

2. THAP1 mutations (DYT6) are an additional cause of early-onset dystonia;Houlden;Neurology,2010

3. A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia;Munchau;Mov Disord,2000

4. DYT6 dystonia: review of the literature and creation of the UMD Locus-Specific Database (LSDB) for mutations in the THAP1 gene;Blanchard;Hum Mutat,2011

5. THAP1 mutations and dystonia phenotypes: genotype phenotype correlations;Xiromerisiou;Mov Disord,2012

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