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

Rossi, Malco; Medina Escobar, Alex; Radrizzani, Martin; Tenembaum, Silvia; Perandones, Claudia; Merello, Marcelo

Rossi, Malco; Medina Escobar, Alex; Radrizzani, Martin; Tenembaum, Silvia; Perandones, Claudia; Merello, Marcelo.

Afiliación

Rossi M; Movement Disorders Section Neuroscience Department Raul Carrea Institute for Neurological Research (FLENI) Buenos Aires Argentina.
Medina Escobar A; Movement Disorders Section Neuroscience Department Raul Carrea Institute for Neurological Research (FLENI) Buenos Aires Argentina.
Radrizzani M; Laboratory of Neuro and Molecular Cytogenetic (CONICET) School of Sciences and Technology CESyMA National University of San Martin Buenos Aires Argentina.
Tenembaum S; Department of Pediatric Neurology National Pediatric Hospital Dr. Juan P. Garrahan Buenos Aires Argentina.
Perandones C; Scientific and Technological Coordination Unit of the ANLIS Directorate National Administration of Laboratories and Institutes of Health, Dr. Carlos G. Malbran Buenos Aires Argentina.
Merello M; Argentine National Scientific and Technological Research Council (CONICET) Buenos Aires Argentina.

Mov Disord Clin Pract ; 4(2): 266-269, 2017.

Article en En | MEDLINE | ID: mdl-30838265

Palabras clave

PEO; POLG; ataxia; dystonia; ophthalmoplegia; scoliosis

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mov Disord Clin Pract Año: 2017 Tipo del documento: Article