Jérémy Raynot

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Nephrotic syndrome of the Finnish type (NSF) is an autosomal-recessive disorder, characterized by massive proteinuria in utero and nephrosis at birth. NSF is caused by mutations in the NPHS1 gene which codes for nephrin [1], a cell adhesion molecule specifically localized at the slit diaphragm of the glomerular basement membrane [2]. Mutations, such as(More)
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