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Article

Renal ApoA-1 amyloidosis with Glu34Lys mutation and intra-amyloid lipid accumulation.

Journal of the American Society of Nephrology : JASN - 1 Dec 2014

Andeen Nicole K, Lam Daniel Y, de Boer Ian H, Nicosia Roberto F

Abstract excerpt

Apolipoprotein A-1 (ApoA-1) amyloidosis occurs as a nonhereditary condition in atherosclerotic plaques, but it can also manifest as a hereditary disorder caused by mutations of the APOA1 gene. Hereditary ApoA-1 amyloidosis presents with diverse organ involvement based on the position of the mutat...

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Source

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Identifiers

PMID: 24925720
DOI: 10.1681/ASN.2013060651
PMCID: PMC4243342

Genes

APOA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24925720-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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