Related Experiment Video
Updated: May 28, 2025

00:06
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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Renal Phenotype Variations among Families with Autosomal Alport Syndrome: Potential Role of Modifier Genes
Abdelrahman Ibrahim1, Edwin Lin2, Mack Hinckley1
1Internal Medicine Department - Nephrology Division, University of Utah Health, Salt Lake City, Utah, USA.
Kidney360
|February 14, 2025
Abstract
No abstract available in PubMed .
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