AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model

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Naziv:	AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
Autori :	Ruizhi Deng; Eva Medico-Salsench; Anita Nikoncuk; Reshmi Ramakrishnan; Kristina Lanko; Nikolas A Kühn; ... et al; Ivan Čapo ; (broj, koautora 52)
Godina:	2023
Publikacija:	ACTA NEUROPATHOLOGICA
ISSN:	0001-6322 Acta Neuropathologica Pretraži identifikator
Tip rezultata:	Naučni članak
Kolacija:	vol. 146 br. 2 str. 353-368
DOI:	10.1007/s00401-023-02579-9
WoS-ID:	000978988700001
Scopus-ID:	2-s2.0-85153927213
PMID:	37119330
PMCID:	PMC10328903
URI:	https://enauka.gov.rs/handle/123456789/828305
Projekat:	China Scholarship Council (CSC) PhD Fellowship [201906300026, 202008500138] Stichting 12q Solve-RD project within the European Rare Disease Models & Mechanisms Network (RDMM-Europe) European Union's Horizon 2020 research and innovation programme Natio
Izvor metapodataka:	(Preuzeto iz Nasi u WoS)
M-kategorija:	21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+

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