De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient-Reference-Cited by-同舟云学术

De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient

Published:2014-04-13 Issue:9 Volume:29 Page:1190-1193
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Dobričić Valerija¹²,Kresojević Nikola¹,Westenberger Ana²,Svetel Marina¹,Tomić Aleksandra¹,Ralić Vesna¹,Petrović Igor¹,Lukić Milica Ječmenica¹,Lohmann Katja²,Novaković Ivana³,Klein Christine²,Kostić Vladimir S.¹

Affiliation:

1. Neurology Clinic CCS; School of Medicine, University of Belgrade; Belgrade Serbia

2. Institute of Neurogenetics, University of Lübeck; Lübeck Germany

3. Institute for Human Genetics, Faculty of Medicine; University of Belgrade; Belgrade Serbia

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25876/fullpdf

Reference23 articles.

1. Mutations in CIZ1 cause adult onset primary cervical dystonia;Xiao;Ann Neurol,2012

2. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis;Charlesworth;Am J Hum Genet,2012

3. Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene;Lohmann;Ann Neurol,2012

4. Mutations in the autoregulatory domain of beta-tubulin 4a cause hereditary dystonia;Hersheson;Ann Neurol,2012

5. Mutations in GNAL cause primary torsion dystonia;Fuchs;Nat Genet,2012

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