Associated Papers
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia.
Wilkinson PA et al.
Brain : a Journal of Neurology, 2004
New insights into the role of CcmC, CcmD and CcmE in the haem delivery pathway during cytochrome c maturation by a complete mutational analysis of the conserved tryptophan-rich motif of CcmC.
Schulz H et al.
Molecular Microbiology, 2000
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