Intra-familial variability of oculoleptomeningeal amyloidosis due to the ATTR I107M (c.381T   >  G) mutation: diagnostic challenges of a rare phenotype

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Source: Amyloid: The Journal of Protein Folding Disorders - September 27, 2023 Category: Biochemistry Authors: Monica AlcantaraVera BrilDepartment of Medicine, Division of Neurology, University of Toronto, Toronto, Canada Source Type: research