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APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal s...

APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal s...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2489601892

APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses

About this item

Full title

APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

Journal title

Pediatric nephrology (Berlin, West), 2021-08, Vol.36 (8), p.2327-2336

Language

English

Formats

Publication information

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

More information

Scope and Contents

Contents

Background
APOL1
high-risk genotypes (HRG) are associated with increased risk of kidney disease in individuals of African ancestry. We analyzed the effects of
APOL1
risk variants on an ethnically diverse Brazilian pediatric nephrotic syndrome (NS) cohort.
Methods
Multicenter study including 318 NS patients, categorized as progress...

Alternative Titles

Full title

APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2489601892

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2489601892

Other Identifiers

ISSN

0931-041X

E-ISSN

1432-198X

DOI

10.1007/s00467-021-04960-w

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