Finnish type of nephrotic syndrome is associated with mutations of which of the following?
Correct Answer: Nephrin
Description: NPHS1 gene mutations = Congenital nephrotic syndrome of the Finnish type, producing a minimal-change disease like glomerulopathy with extensive foot process effacement. NPHS1 is located on chromosome 19q13 and encodes the protein nephrin.
Category:
Pathology
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