Clinical Trial Update: Natural History Study of Patients with HPDL Mutations

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Summary

This is an ongoing natural history study of individuals with HPDL mutations to document clinical features and disease progression.

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Diseases / indications

• Hereditary Spastic Paraplegia
• Mitochondrial Encephalomyopathies

Snippet

Sponsor: University of California, San Diego | Conditions: Mitochondrial Encephalomyopathies, Hereditary Spastic Paraplegia | Status: RECRUITING