About Lissencephaly due to LIS1 mutation
Lissencephaly due to LIS1 mutation is a rare disease catalogued by Orphanet (ORPHA:95232). It is associated with the PAFAH1B1 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 Lissencephaly due to LIS1 mutation trials.
Search ClinicalTrials.gov for "Lissencephaly due to LIS1 mutation" or filter by Orphanet code ORPHA:95232 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 Lissencephaly due to LIS1 mutation trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Lissencephaly due to LIS1 mutation. Updated daily.