spastic paraplegia type-7
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Genetics
- autosomal recessive
- associated with paraplegin mutations
See hereditary spastic paraplegia
More general terms
References
- ↑ Casari G et al. Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. Cell 93:973-83, 1998 PMID: https://www.ncbi.nlm.nih.gov/pubmed/9635427