Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
- 1 May 2002
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 70 (5), 1328-1332
- https://doi.org/10.1086/339935
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaNature Genetics, 2001
- Recent advances in hereditary spastic paraplegiaCurrent Opinion in Neurology, 2001
- Molecular basis of inherited spastic paraplegiasCurrent Opinion in Genetics & Development, 2001
- The Importance of a Mobile Loop in Regulating Chaperonin/ Co-chaperonin InteractionJournal of Biological Chemistry, 2001
- AAA proteases: cellular machines for degrading membrane proteinsTrends in Biochemical Sciences, 2000
- A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34American Journal of Human Genetics, 2000
- Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiaNature Genetics, 1999
- Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial MetalloproteaseCell, 1998
- Effects of Two Mutations Detected in Medium Chain Acyl-CoA Dehydrogenase (MCAD)-deficient Patients on Folding, Oligomer Assembly, and Stability of MCAD EnzymePublished by Elsevier ,1995
- The groES and groEL heat shock gene products of Escherichia coli are essential for bacterial growth at all temperaturesJournal of Bacteriology, 1989