About PMP22-RAI1 contiguous gene duplication syndrome
PMP22-RAI1 contiguous gene duplication syndrome is a rare disease catalogued by Orphanet (ORPHA:477817). It is associated with the RAI1 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 PMP22-RAI1 contiguous gene duplication syndrome trials.
Search ClinicalTrials.gov for "PMP22-RAI1 contiguous gene duplication syndrome" or filter by Orphanet code ORPHA:477817 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 PMP22-RAI1 contiguous gene duplication syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for PMP22-RAI1 contiguous gene duplication syndrome. Updated daily.