Reply to: 'Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion'

Autor:	Aurora Pujol, M. Urtasun, Montserrat Ruiz, Ivonne Jericó, Gorka Fernández-Eulate, Raquel Saez-Villaverde, Victoria Alvarez, Uxoa Fernández-Pelayo, Agatha Schlüter, Josep Gamez, Jon Infante, Ander Olaskoaga, Raúl Barahona-Hernando, E. Solà, Miren Zulaica, Elena Martínez-Sáez, José Luis Muñoz-Blanco, Mikel Muñoz-Oreja, Germán Morís, Antonella Spinazzola, Beatriz De la Casa-Fages, Victoria Zelaya, Francisco Grandas, Ian J Holt, Irene Catalina, Adolfo López de Munain, María García-Barcina
Rok vydání:	2019
Předmět:	Genetics Paraplegia Paraplegin Spastic Paraplegia Hereditary Parkinsonism MtDNA depletion Metalloendopeptidases Biology medicine.disease DNA Mitochondrial AAA proteins Neurology Parkinsonian Disorders medicine ATPases Associated with Diverse Cellular Activities Humans Neurology (clinical)
Zdroj:	Movement disorders : official journal of the Movement Disorder SocietyReferences. 34(12)
ISSN:	1531-8257
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e53523f6112e4397ac1fa6593b597e08 https://pubmed.ncbi.nlm.nih.gov/31845759 Zobrazit plný text záznamu Plný text