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Article

COQ8B nephropathy: Early detection and optimal treatment.

Molecular genetics & genomic medicine - 1 Aug 2020

Song Xiaoxiang, Fang Xiaoyan, Tang Xiaoshan, Cao Qi, Zhai Yihui, Chen Jing, Liu Jialu, Zhang Zhiqing, Xiang Tianchao, Qian Yanyan, Wu Bingbing, Wang Huijun, Zhou Wenhao, Liu Cuihua, Shen Qian, Xu Hong, Rao Jia

Abstract excerpt

BACKGROUND: Mutations in COQ8B (*615567) as a defect of coenzyme Q10 (CoQ10) cause steroid resistant nephrotic syndrome (SRNS). METHODS: To define the clinical course and prognosis of COQ8B nephropathy, we retrospectively assessed the genotype and phenotype in patients with COQ8B mutations from Chinese Children Genetic Kidney Disease Database. We performed the comparing study of renal outcome following CoQ10...

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PMID: 32543055
DOI: 10.1002/mgg3.1360
PMCID: PMC7434746

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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