Screening of mutations inGNALin sporadic dystonia patients
Author:
Affiliation:
1. Institute of Medical Genetics and Applied Genomics, Rare Disease Center Tuebingen; University of Tuebingen; Tuebingen Germany
2. Transgenic Facility Tuebingen; University of Tuebingen; Tuebingen Germany
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference12 articles.
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3. Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis;Phukan;Lancet Neurol,2011
4. Mutations in CIZ1 cause adult onset primary cervical dystonia;Xiao;Ann Neurol,2012
5. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis;Charlesworth;Am J Hum Genet,2012
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