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Article

Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis.

Human genomics - 12 Nov 2022

Hussain Hafiz Muhammad Jafar, Cai Yikai, Weng Qinjie, Tong Jun, Aftab Ayesha, Jin Yuanmeng, Liu Jian, Yu Shuwen, Fang Zhengying, Du Wen, Pan Xiaoxia, Ren Hong, Xie Jingyuan

Abstract excerpt

BACKGROUND: Focal and segmental glomerulosclerosis (FSGS) is a histological pathology that characterizes a wide spectrum of diseases. Many genes associated with FSGS have been studied previously, but there are still some FSGS families reported in the literature without the identification of known gene mutations. The aim of this study was to investigate the new genetic cause of adult-onset FSGS. METHODS: This...

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Identifiers

PMID: 36371311
DOI: 10.1186/s40246-022-00430-y
PMCID: PMC9655905

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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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