Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia

Miranda, Marcelo; Harmuth, Florian; Bustamante, M Leonor; Rossi, Malco Damián; Sturm, Marc; Magnusson, Ólafur Th.; Bauer, Peter; Klockgether, Thomas; Ramirez, Alfredo

dc.contributor.author	Miranda, Marcelo
dc.contributor.author	Harmuth, Florian
dc.contributor.author	Bustamante, M Leonor
dc.contributor.author	Rossi, Malco Damián
dc.contributor.author	Sturm, Marc
dc.contributor.author	Magnusson, Ólafur Th.
dc.contributor.author	Bauer, Peter
dc.contributor.author	Klockgether, Thomas
dc.contributor.author	Ramirez, Alfredo
dc.date.accessioned	2021-04-28T16:20:47Z
dc.date.available	2021-04-28T16:20:47Z
dc.date.issued	2020-12
dc.identifier.citation	Miranda, M., Harmuth, F., Bustamante, M.L., Rossi, M.D., Sturm, M., Magnusson, Ó.T., Bauer, P., Klockgether, T., Ramirez, A., 2020. Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia. Parkinsonism Relat Disord 81, 45-47. https://doi.org/10.1016/j.parkreldis.2020.10.004	es_ES
dc.identifier.uri	https://repositorio.fleni.org.ar/xmlui/handle/123456789/440
dc.identifier.uri	https://doi.org/10.1016/j.parkreldis.2020.10.004
dc.language.iso	eng	es_ES
dc.publisher	Elsevier Science	es_ES
dc.rights	info:eu-repo/semantics/openAccess
dc.rights.uri	https://creativecommons.org/licenses/by/2.5/ar/
dc.subject	Enfermedad de Parkinson	es_ES
dc.subject	Parkinson Disease	es_ES
dc.title	Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia	es_ES
dc.type	info:eu-repo/semantics/article	es_ES
dc.type	info:eu-repo/semantics/publishedVersion
dc.description.fil	Fil: Rossi, Malco Damián. Fleni. Departamento de Neurología. Servicio de Movimientos Anormales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina.
dc.description.fil	Fil: Miranda, Marcelo. Fundación Diagnosis; Chile. Clinica Las Condes. Department of Neurology; Chile.
dc.description.fil	Fil: Harmuth, Florian. University of Tuebingen. Institute of Medical Genetics and Applied Genomics; Alemania.
dc.description.fil	Fil: Bustamante, M Leonor. Fundación Diagnosis; Chile. University of Chile. Faculty of Medicine. Biomedical Sciences Institute. Human Genetics Program; Chile. University of Chile. Faculty of Medicine. Department of Psychiatry and Mental Health, North Division; Chile.
dc.description.fil	Fil: Sturm, Marc. University of Tuebingen. Institute of Medical Genetics and Applied Genomics; Alemania.
dc.description.fil	Fil: Magnusson, Ólafur Th. eCODE Genetics; Islandia.
dc.description.fil	Fil: Bauer, Peter. University of Tuebingen. Institute of Medical Genetics and Applied Genomics; Alemania.
dc.description.fil	Fil: Klockgether, Thomas. University of Bonn. Department of Neurology; Alemania. German Center for Neurodegenerative Diseases (DZNE); Alemania.
dc.description.fil	Fil: Ramirez, Alfredo. German Center for Neurodegenerative Diseases (DZNE); Alemania. University of Bonn. Department of Neurodegenerative Diseases and Geriatric Psychiatry; Alemania. University of Cologne. Department of Psychiatry and Psychotherapy. Division of Neurogenetics and Molecular Psychiatry; Alemania.
dc.relation.ispartofVOLUME	81
dc.relation.ispartofPAGINATION	45-47
dc.relation.ispartofCOUNTRY	Estados Unidos
dc.relation.ispartofCITY	Nueva York
dc.relation.ispartofTITLE	Parkinsonism & related disorders.
dc.relation.ispartofISSN	1873-5126
dc.type.snrd	info:ar-repo/semantics/artículo	es_ES