About Angelman syndrome due to paternal uniparental disomy of chromosome 15
Angelman syndrome due to paternal uniparental disomy of chromosome 15 is a rare disease catalogued by Orphanet (ORPHA:98795). It is associated with the UBE3A 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 Angelman syndrome due to paternal uniparental disomy of chromosome 15 trials.
Search ClinicalTrials.gov for "Angelman syndrome due to paternal uniparental disomy of chromosome 15" or filter by Orphanet code ORPHA:98795 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 Angelman syndrome due to paternal uniparental disomy of chromosome 15 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Angelman syndrome due to paternal uniparental disomy of chromosome 15. Updated daily.