New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosis.
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DOI: 10.1016/j.kint.2020.03.033
Abstract: Apolipoprotein A1 amyloidosis (ApoAI) results from specific mutations in the APOA1 gene causing abnormal accumulation of amyloid fibrils in diverse tissues. The kidney is a prominent target tissue in ApoAI amyloidosis with a remarkable selectivity… read more here.
Keywords: new clinical; apoa amyloid; apoai amyloidosis; amyloidosis ... See more keywords