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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_198fa89aeaa74b68ad05062bbd9ba8e0

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

About this item

Full title

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

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2023-01, Vol.13 (1), p.805-805, Article 805

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

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. Clin...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_198fa89aeaa74b68ad05062bbd9ba8e0

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_198fa89aeaa74b68ad05062bbd9ba8e0

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-022-26291-y

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