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. |
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| 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 |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2330-1619 |
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| DOI: | 10.1002/mdc3.13740 |
