QuickView for SPG7;jsessionid=00ED0D8B2187AE703BD3F84A567A414E (gene)

1. Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spast…
2. Early Onset Degenerative Parkinsonism - Consider SPG7 Mutation.
3. SARM1 deletion delays cerebellar but not spinal cord degeneration in an enhanced mouse model of SPG7…
4. A novel compound heterozygous SPG7 variant is associated with progressive spastic ataxia and persecu…
5. SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.

There were no clinical trials for SPG7;jsessionid=00ED0D8B2187AE703BD3F84A567A414E