J. Hansen

Grp78 Is Involved in Retention of Mutant Low Density Lipoprotein Receptor Protein in the Endoplasmic Reticulum*

L. Bolund, P. Bross, O. Jensen, 2000, The Journal of Biological Chemistry.

Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential

Huanming Yang, L. Bolund, Zhijie Li, 2006, Journal of Human Genetics.

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60.

A. Dürr, A. Brice, C. Georgopoulos, 2002, American journal of human genetics.

Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter

Anders D. Børglum, Lars Bolund, Karsten Kristiansen, 2002, Human Genetics.

Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter

Anders D. Børglum, Lars Bolund, Karsten Kristiansen, 2003, Human Genetics.