NEPHRONOPHTHISIS 13

Known as: NPHP13 
 
National Institutes of Health

Papers overview

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2015
2015
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 (HRFCDs) are a group of monogenic disorders characterized by developmental abnormalities… (More)
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