About Gamma-aminobutyric acid transaminase deficiency
Gamma-aminobutyric acid transaminase deficiency is a rare disease catalogued by Orphanet (ORPHA:2066). It is associated with the ABAT 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 Gamma-aminobutyric acid transaminase deficiency trials.
Search ClinicalTrials.gov for "Gamma-aminobutyric acid transaminase deficiency" or filter by Orphanet code ORPHA:2066 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 Gamma-aminobutyric acid transaminase deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Gamma-aminobutyric acid transaminase deficiency. Updated daily.