TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study

BACKGROUND: Parkinsonian features have been described in patients harboring variants in nuclear genes encoding for proteins involved in mitochondrial DNA maintenance, such as TWNK. OBJECTIVES: The aim was to screen for TWNK variants in an Italian cohort of Parkinson's disease (PD) patients and...

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Detalles Bibliográficos
Autores principales: Percetti, Marco, Franco, Giulia, Monfrini, Edoardo, Caporali, Leonardo, Minardi, Raffaella, La Morgia, Chiara, Valentino, Maria Lucia, Liguori, Rocco, Palmieri, Ilaria, Ottaviani, Donatella, Vizziello, Maria, Ronchi, Dario, Di Berardino, Federica, Cocco, Antoniangela, Macao, Bertil, Falkenberg, Maria, Comi, Giacomo Pietro, Albanese, Alberto, Giometto, Bruno, Valente, Enza Maria, Carelli, Valerio, Di Fonzo, Alessio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Regular Issue Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544864/
https://www.ncbi.nlm.nih.gov/pubmed/35792653
http://dx.doi.org/10.1002/mds.29139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544864/
https://www.ncbi.nlm.nih.gov/pubmed/35792653
http://dx.doi.org/10.1002/mds.29139

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