Clinical and molecular characterization of a large primary hyperoxaluria cohort from Saudi Arabia: a retrospective study.

Majid AlfadhelMuhammad UmairMalak A AlghamdiKhalid Al FakeehAbdullah T Al QahtaniAfrah FarahatMohamed A ShalabyJameela A KariRupesh RainaPierre CochatKhalid A Alhasan

Published in: Pediatric nephrology (Berlin, Germany) (2022)

Characterization of the genetic and clinical aspects of PH in this unique population provides direction for improved patient management and further research. A higher resolution version of the Graphical abstract is available as Supplementary information.

Keyphrases

saudi arabia
case report
dna methylation
copy number
social media