About Autosomal recessive spastic paraplegia type 43
Autosomal recessive spastic paraplegia type 43 is a rare disease catalogued by Orphanet (ORPHA:320370). It is associated with the C19ORF12 gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Autosomal recessive spastic paraplegia type 43 trials.
Search ClinicalTrials.gov for "Autosomal recessive spastic paraplegia type 43" or filter by Orphanet code ORPHA:320370 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Autosomal recessive spastic paraplegia type 43 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal recessive spastic paraplegia type 43. Updated daily.