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Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain.

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Title: Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain.
Authors: Baviera-Muñoz R; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain., Carretero-Vilarroig L; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cavanilles Institute of Biodiversity and Evolutionary University of Valencia Valencia Spain., Muelas N; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Department of Medicine University of Valencia Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain., Sivera R; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.; Department of Medicine University CEU Cardenal Herrera Valencia Spain., Sopena-Novales P; Nuclear Medicine Department Hospital Universitari I Politècnic La Fe Valencia Spain., Martínez-Sanchis B; Nuclear Medicine Department Hospital Universitari I Politècnic La Fe Valencia Spain., Sastre-Bataller I; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain., Campins-Romeu M; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain., Martínez-Torres I; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain., García-Verdugo JM; Cavanilles Institute of Biodiversity and Evolutionary University of Valencia Valencia Spain., Millán JM; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain., Jaijo T; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.; Department of Genetics Hospital Universitari I Politècnic La Fe Valencia Spain., Aller E; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.; Department of Genetics Hospital Universitari I Politècnic La Fe Valencia Spain., Bataller L; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Department of Medicine University of Valencia Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.
Source: Movement disorders clinical practice [Mov Disord Clin Pract] 2023 May 05; Vol. 10 (6), pp. 992-997. Date of Electronic Publication: 2023 May 05 (Print Publication: 2023).
Publication Type: Journal Article
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101630279 Publication Model: eCollection Cited Medium: Internet ISSN: 2330-1619 (Electronic) Linking ISSN: 23301619 NLM ISO Abbreviation: Mov Disord Clin Pract Subsets: PubMed not MEDLINE
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  Data: Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain.
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  Data: <searchLink fieldCode="AU" term="%22Baviera-Muñoz+R%22">Baviera-Muñoz R</searchLink>; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Carretero-Vilarroig+L%22">Carretero-Vilarroig L</searchLink>; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cavanilles Institute of Biodiversity and Evolutionary University of Valencia Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Muelas+N%22">Muelas N</searchLink>; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Department of Medicine University of Valencia Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.<br /><searchLink fieldCode="AU" term="%22Sivera+R%22">Sivera R</searchLink>; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.; Department of Medicine University CEU Cardenal Herrera Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Sopena-Novales+P%22">Sopena-Novales P</searchLink>; Nuclear Medicine Department Hospital Universitari I Politècnic La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Martínez-Sanchis+B%22">Martínez-Sanchis B</searchLink>; Nuclear Medicine Department Hospital Universitari I Politècnic La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Sastre-Bataller+I%22">Sastre-Bataller I</searchLink>; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Campins-Romeu+M%22">Campins-Romeu M</searchLink>; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Martínez-Torres+I%22">Martínez-Torres I</searchLink>; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22García-Verdugo+JM%22">García-Verdugo JM</searchLink>; Cavanilles Institute of Biodiversity and Evolutionary University of Valencia Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Millán+JM%22">Millán JM</searchLink>; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.<br /><searchLink fieldCode="AU" term="%22Jaijo+T%22">Jaijo T</searchLink>; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.; Department of Genetics Hospital Universitari I Politècnic La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Aller+E%22">Aller E</searchLink>; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Cellular, Molecular and Genomics Biomedicine Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.; Department of Genetics Hospital Universitari I Politècnic La Fe Valencia Spain.<br /><searchLink fieldCode="AU" term="%22Bataller+L%22">Bataller L</searchLink>; Neurology Department Hospital Universitari I Politècnic La Fe Valencia Spain.; Neuromuscular and Ataxias Research Group Instituto de Investigación Sanitaria La Fe Valencia Spain.; Rare Diseases Joint Unit CIPF-IIS La Fe Valencia Spain.; Department of Medicine University of Valencia Valencia Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras U755, U763, (CIBERER) Madrid Spain.
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  Data: <searchLink fieldCode="JN" term="%22101630279%22">Movement disorders clinical practice</searchLink> [Mov Disord Clin Pract] 2023 May 05; Vol. 10 (6), pp. 992-997. <i>Date of Electronic Publication: </i>2023 May 05 (<i>Print Publication: </i>2023).
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