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

Monica AlcantaraDepartment of Medicine, Division of Neurology, University of Toronto, Toronto, CanadaView further author information

Vera BrilDepartment of Medicine, Division of Neurology, University of Toronto, Toronto, CanadaCorrespondence[email protected]
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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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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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