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nephrotic syndrome, type 1
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NPHS1
Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.
Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type.
CD2AP is expressed with nephrin in developing podocytes and is found widely in mature kidney and elsewhere.
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External
Lymphocyte Markers As Predictors Of Responsiveness To Rituximab Among Patients With Idiopathic Nephrotic Syndrome