Skip to search formSkip to main contentSkip to account menu

NEPHRONOPHTHISIS 13

Known as: NPHP13 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal recessive inheritanceChronic kidney disease stage 5WDR19 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney
BackgroundNephronophthisis 13 (NPHP 13) is associated with mutations in the WDR19 gene, which encodes for a protein in the… 
2015
2015
Hepatorenal fibrocystic diseases in children
BackgroundHepatorenal fibrocystic diseases (HRFCDs) are a group of monogenic disorders characterized by developmental… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)