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Article

Hereditary features, treatment, and prognosis of the lipoprotein glomerulopathy in patients with the APOE Kyoto mutation.

Kidney international - 1 Feb 2014

Hu Zhangxue, Huang Songmin, Wu Yu, Liu Yunqiang, Liu Xiaoxia, Su Dan, Tao Ye, Fu Ping, Zhang Xiuhui, Peng Ziying, Zhang Sizhong, Yang Yuan

Abstract excerpt

Lipoprotein glomerulopathy is a rare inherited renal disease, caused by mutation of the APOE gene, characterized by proteinuria and nephrotic syndrome with elevated serum apoE. Since its treatment and outcome are unknown, we retrospectively studied 35 patients within 31 unrelated Han families with biopsy-proven lipoprotein glomerulopathy residing in the same county in southwest China. DNA sequencing detected the...

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Source

Identifiers

PMID: 24025644
DOI: 10.1038/ki.2013.335

Genes

APOE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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Hereditary features, treatment, and prognosis of the lipoprotein glomerulopathy in patients with the APOE Kyoto mutation.PMID 24025644Read ↗

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