Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias-Reference-Cited by-同舟云学术

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Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias

Published:2004-05-26 Issue:11 Volume:19 Page:1294-1297
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Grundmann Kathrin,Laubis-Herrmann Ulrike,Dressler Dirk,Vollmer-Haase Juliane,Bauer Peter,Stuhrmann Manfred,Schulte Thorsten,Schöls Ludger,Topka Helge,Riess Olaf

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference29 articles.

1. Concept and classification of dystonia;Fahn;Adv Neurol,1988

2. Dystonia: clinical features, genetics, and treatment;Klein;Curr Opin Neurol,2002

3. The genetics of primary dystonias and related disorders;Nemeth;Brain,2002

4. Classification of dystonia;Fahn;Adv Neurol,1998

5. A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia;Slominsky;Hum Mutat,1999

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Twenty years on: Myoclonus‐dystonia and ε‐sarcoglycan — neurodevelopment, channel, and signaling dysfunction;Movement Disorders;2019-08-26

2. Genetic evaluation in hereditary dystonia;Handbook of Dystonia;2012-05

3. Novel THAP1 sequence variants in primary dystonia;Neurology;2010-01-18

4. High-throughput mutational analysis of TOR1A in primary dystonia;BMC Medical Genetics;2009-03-11

5. Dystonia: Myoclonus–Dystonia;Encyclopedia of Neuroscience;2009

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