Dystonia in a Patient with Autosomal-Dominant Progressive External Ophthalmoplegia Type 1 Caused by Mutation in the POLG Gene

dc.creatorRossi, Malco
dc.creatorMedina Escobar, Alex
dc.creatorRadrizzani, Martin
dc.creatorTenembaum, Silvia
dc.creatorPerandones, Claudia
dc.creatorMerello, Marcelo
dc.date2020-05-17T22:47:31Z
dc.date2020-05-17T22:47:31Z
dc.date2017
dc.date.accessioned2023-08-29T20:06:50Z
dc.date.available2023-08-29T20:06:50Z
dc.identifierhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353407/
dc.identifierhttp://sgc.anlis.gob.ar/handle/123456789/1576
dc.identifier10.1002/mdc3.12397
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8519338
dc.languageen
dc.relationMovement disorders clinical practice
dc.rightsopen
dc.subjectAtaxia
dc.subjectEscoliosis
dc.subjectOftalmoplejía
dc.titleDystonia in a Patient with Autosomal-Dominant Progressive External Ophthalmoplegia Type 1 Caused by Mutation in the POLG Gene
dc.typeArtículo


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