Review summarizes pathogenesis and therapeutic frontiers in kidney amyloidosis, highlighting distinct protein distributions across disease forms.
Amyloidosis includes a diverse group of rare diseases characterized by the misfolding of native or mutant proteins, leading to extracellular accumulation in various organs. While 42 proteins have been identified to date, their distribution differs between systemic and localized forms.
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Cervantes et al. (2024) studied this question.
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