NEPHRONOPHTHISIS 13

Known as: NPHP13 
 
National Institutes of Health

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3 relations
Autosomal recessive inheritanceChronic kidney disease stage 5WDR19 gene

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2015
2015
Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney
Nephronophthisis 13 (NPHP 13) is associated with mutations in the WDR19 gene, which encodes for a protein in the intraflagellar… (More)
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2015
2015
Hepatorenal fibrocystic diseases in children
Hepatorenal fibrocystic diseases (HRFCDs) are a group of monogenic disorders characterized by developmental abnormalities… (More)
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