Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls-Reference-Cited by-同舟云学术

Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls

Published:2013-10-22 Issue:1 Volume:29 Page:143-147
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Zech Michael¹²,Gross Nadine¹,Jochim Angela¹,Castrop Florian¹,Kaffe Maria¹²,Dresel Christian¹,Lichtner Peter²³,Peters Annette⁴,Gieger Christian⁵,Meitinger Thomas²³,Haslinger Bernhard¹,Winkelmann Juliane¹²³⁶⁷

Affiliation:

1. Neurologische Klinik und Poliklinik; Klinikum rechts der Isar; Technische Universität München; Munich Germany

2. Institut für Humangenetik; Helmholtz Zentrum München Munich Germany

3. Institut für Humangenetik, Technische Universität München; Munich Germany

4. Institute of Epidemiology II; Helmholtz Zentrum München Munich Germany

5. Institute of Genetic Epidemiology; Helmholtz Zentrum München Munich Germany

6. Department of Neurology and Neurological Sciences; Stanford University School of Medicine; Palo Alto California USA

7. Munich Cluster for Systems Neurology; SyNergy Munich Germany

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference22 articles.

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2. Clinical and genetic evaluation in a French population presenting with primary focal dystonia;Dhaenens;Mov Disord,2005

3. Focal and segmental primary dystonia in north-western Germany-a clinico-genetic study;Maniak;Acta Neurol Scand,2003

4. A genetic study of idiopathic focal dystonias;Waddy;Ann Neurol,1991

5. Genetic and clinical features of primary torsion dystonia;Ozelius;Neurobiol Dis,2011

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