This study focuses on hereditary transthyretin amyloidosis (ATTRv) with the Val50Met variant in a non endemic aerea
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Describe the phenotypic variables (preclinical, cardiological, neurological and mixed) in patients carrying the TTR Val50Met variant in a non-endemic population.
Timeframe: 2 years