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

Bross, 1995, Effects of two mutations detected in medium chain acyl-CoA dehydrogenase (MCAD)-deficient patients on folding, oligomer assembly, and stability of MCAD enzyme, J Biol Chem, 270, 10284, 10.1074/jbc.270.17.10284

Casari, 1998, Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease, Cell, 93, 973, 10.1016/S0092-8674(00)81203-9

Casari, 2001, Molecular basis of inherited spastic paraplegias, Curr Opin Genet Dev, 11, 336, 10.1016/S0959-437X(00)00199-4

Castanie, 1997, A set of pBR322-compatible plasmids allowing the testing of chaperone-assisted folding of proteins overexpressed in Escherichia coli, Anal Biochem, 254, 150, 10.1006/abio.1997.2423

Fayet, 1989, The groES and groEL heat shock gene products of Escherichia coli are essential for bacterial growth at all temperatures, J Bacteriol, 171, 1379, 10.1128/jb.171.3.1379-1385.1989

Fontaine, 2000, A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34, Am J Hum Genet, 66, 702, 10.1086/302776

Hazan, 1999, Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia, Nat Genet, 23, 296, 10.1038/15472

Langer, 2000, AAA proteases: cellular machines for degrading membrane proteins, Trends Biochem Sci, 25, 247, 10.1016/S0968-0004(99)01541-8

Richardson, 2001, The importance of a mobile loop in regulating chaperonin/co-chaperonin interaction: humans versus Escherichia coli, J Biol Chem, 276, 4981, 10.1074/jbc.M008628200

Slavotinek, 2001, Unfolding the role of chaperones and chaperonins in human disease, Trends Genet, 17, 528, 10.1016/S0168-9525(01)02413-1

Tallaksen, 2001, Recent advances in hereditary spastic paraplegia, Curr Opin Neurol, 14, 457, 10.1097/00019052-200108000-00005

Xu, 1997, The crystal structure of the asymmetric GroEL-GroES-(ADP)7 chaperonin complex, Nature, 388, 741, 10.1038/41944

Zhao, 2001, Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia, Nat Genet, 29, 326, 10.1038/ng758