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Alexandre Terré1,2, David Buob3, Alexandre Cez4

  • 1Department of Internal Medicine, National Reference Center for Autoinflammatory Diseases and AA amyloidosis, Assistance Publique-Hôpitaux de Paris, Tenon Hospital, Sorbonne University, Paris, France.

British Journal of Haematology
|March 11, 2024
PubMed
Abstract

No abstract available in PubMed .

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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
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