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Publications by Marit Nyholm Nielsen

Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

American Journal of Human Genetics

English

The Hsp60-(p.V98I) Mutation Associated With Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Bothin Vitroandin Vivo

Journal of Biological Chemistry

Molecular Biology

English