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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

Amyloid(2023)

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Click to increase image sizeClick to decrease image size Informed consentWe confirm that the subject involved in this report provided informed consent.Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThe author(s) reported there is no funding associated with the work featured in this article.
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