Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy

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Title:	Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy
Authors :	Armirola-Ricaurte, Camila; ...; Tomic, Aleksandra; ...; Milic-Rasic, Vedrana; (broj, koautora 20)
Issue Date:	2025
Publication:	BRAIN
ISSN:	0006-8950 Brain Search Idenfier
Type:	Article
Collation:	vol. 149 br. 1 str. 178-193
DOI:	10.1093/brain/awaf300
WoS-ID:	001650733600001
Scopus-ID:	2-s2.0-105027121337
URI:	https://enauka.gov.rs/handle/123456789/1023049
Project:	Association Belge contre les Maladies Neuromusculaires' French Muscular Dystrophy Association [23708] European Union Seventh Framework Programme [FP7/2007-2013, 305444] Muscular Dystrophy Association [MDA510281] the National Institute for Health Research University College London Hospitals Biomedical Research Centre National Institutes of Neurological Diseases and Stroke and office of Rare Diseases [U54NS065712, 1UOINS109403-01] Charcot Marie Tooth Association Medical Research Council [MRC MR/S005021/1] Research Fund of the University of Antwerp Harrington Discovery Institute European Union's Horizon 2020 research and innovation programme [779257] Fund for Scientific Research [G048220N, G0A2122N] Wellcome Trust [G104817]
Metadata source:	(Preuzeto iz Nasi u WoS)
M-category:	21a+M21a+

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