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收藏Mitochondrial Hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy
Magen, Daniella; Georgopoulos, Costa; Bross, Peter; Ang, Debbie; Segev, Yardena; Goldsher, Dorit; Nemirovski, Alexandra; Shahar, Eli; Ravid, Sarit; Luder, Anthony; Heno, Bayan; Gershoni-Baruch, Ruth; Skorecki, Karl; Mandel, Hanna
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收藏The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo
Bross, Peter; Naundrup, Soren; Hansen, Jakob; Nielsen, Marit Nyholm; Christensen, Jane Hvarregaard; Kruhoffer, Mogens; Palmfeldt, Johan; Corydon, Thomas Juhl; Gregersen, Niels; Ang, Debbie; Georgopoulos, Costa; Nielsen, Kare Lehmann
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收藏Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60
Hansen, JJ; Dürr, A; Cournu-Rebeix, I; Georgopoulos, C; Ang, D; Nielsen, MN; Davoine, CS; Brice, A; Fontaine, B; Gregersen, N; Bross, P
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