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Article

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.

Scientific reports - 14 Jan 2020

Nagano China, Yamamura Tomohiko, Horinouchi Tomoko, Aoto Yuya, Ishiko Shinya, Sakakibara Nana, Shima Yuko, Nakanishi Koichi, Nagase Hiroaki, Iijima Kazumoto, Nozu Kandai

Abstract excerpt

Numerous disease-causing gene mutations have been identified in proteinuric diseases, such as nephrotic syndrome and glomerulosclerosis. This report describes the results of comprehensive genetic diagnosis of Japanese patients with severe proteinuria. In addition, the report describes the clinical characteristics of patients with monogenic disease-causing mutations. We conducted comprehensive gene screening of...

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Share to Glomerular Filtration Rate
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31937884
DOI: 10.1038/s41598-019-57149-5
PMCID: PMC6959278

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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