Kidney-differentiated cells derived from Lowe Syndrome patient’s iPSCs show ciliogenesis defects and Six2 retention at the Golgi complex
Author:
Funder
National Institutes of Health
Lowe Syndrome Trust
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference71 articles.
1. The oculocerebrorenal syndrome of Lowe: an update;A Bokenkamp;Pediatr Nephrol,2016
2. Lowe syndrome;M Loi;Orphanet J Rare Dis,2006
3. Renal phenotype in Lowe Syndrome: a selective proximal tubular dysfunction;D Bockenhauer;Clin J Am Soc Nephrol,2008
4. Fanconi or not Fanconi? Lowe syndrome revisited;R Kleta;Clin J Am Soc Nephrol,2008
5. The Lowe syndrome protein OCRL1 is involved in primary cilia assembly;BG Coon;Hum Mol Genet,2012
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