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eNauka >  Results >  AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
Title: AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
Authors Ruizhi Deng; Eva Medico-Salsench; Anita Nikoncuk; Reshmi Ramakrishnan; Kristina Lanko; Nikolas A Kühn; ... et al; Ivan Čapo  ; (broj, koautora 52)
Issue Date: 2023
Publication: ACTA NEUROPATHOLOGICA
ISSN: 0001-6322 Acta Neuropathologica Search Idenfier
Type: Article
Collation: 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
Project: 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
Metadata source: (Preuzeto iz Nasi u WoS)
M-category: 
21aM21a

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