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Article

Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis.

Scientific reports - 16 Jan 2023

Isaranuwatchai Suramath, Chanakul Ankanee, Ittiwut Chupong, Ittiwut Rungnapa, Srichomthong Chalurmpon, Shotelersuk Vorasuk, Suphapeetiporn Kanya, Praditpornsilpa Kearkiat

Abstract excerpt

The spectra of underlying genetic variants for various clinical entities including focal segmental glomerulosclerosis (FSGS) vary among different populations. Here we described the clinical and genetic characteristics of biopsy-proven FSGS patients in Thailand. Patients with FSGS pathology, without secondary causes, were included in our study. Clinical laboratory and pathological data were collected. Whole-exome...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 36646731
DOI: 10.1038/s41598-022-26291-y
PMCID: PMC9842604

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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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