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COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2401808687

COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

About this item

Full title

COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

Journal title

Pediatric nephrology (Berlin, West), 2020-10, Vol.35 (10), p.1941-1952

Language

English

Formats

Publication information

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

More information

Scope and Contents

Contents

Background
Alport syndrome (AS) is an inherited glomerular disease caused by mutations in
COL4A3
,
COL4A4
, or
COL4A5
. Associations between clinical manifestations and genotype are not yet well defined. Our study aimed to define clinical and genetic characteristics, establish genotype–phenotype correlations, and determine prog...

Alternative Titles

Full title

COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2401808687

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2401808687

Other Identifiers

ISSN

0931-041X

E-ISSN

1432-198X

DOI

10.1007/s00467-020-04574-8

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