Dystonia (DYT) genetic loci
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Reference33 articles.
1. Human gene for torsion dystonia located on chromosome 9q32–q34;Ozelius;Neuron,1989
2. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein;Ozelius;Nat Genet,1997
3. Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34;Kramer;Ann Neurol,1990
4. Natural history of idiopathic torsion dystonia;Marsden;Adv Neurol,1976
5. Autosomal recessive, DYT2-like primary torsion dystonia: a new family;Khan;Neurology,2003
Cited by 8 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. Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome;Neuroscience Letters;2019-06
2. A novel SGCE gene mutation in a Moroccan sporadic case with myoclonus-dystonia syndrome;Gene Reports;2018-06
3. DYT1 Generalized Dystonia;Current Clinical Neurology;2012
4. Role of DYT1 gene in early-onset primary torsion dystonia;NEURAL REGEN RES;2010
5. Myoclonus in fraternal twin toddlers: A French family with a novel mutation in the SGCE gene;European Journal of Paediatric Neurology;2009-11
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