Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression

Overview of attention for article published in Orphanet Journal of Rare Diseases, October 2021

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Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression https://t.co/uQu9ff8iid

Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression https://t.co/gulYxJYam4

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