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NTIS 바로가기The FEBS journal, v.282 no.11, 2015년, pp.2076 - 2088
Seirafi, Marjan (Department of Biochemistry and the Groupe de Recherche axé) , Kozlov, Guennadi (sur la Structure des Proté) , Gehring, Kalle (ines, McGill University Montré)
Mutations in the parkin or PINK1 genes are the leading cause of the autosomal recessive form of Parkinson’s disease. The gene products, the E3 ubiquitin ligase parkin and the serine/threonine kinase PINK1, are neuroprotective proteins, which act together in a mitochondrial quality control pathway. H...
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