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Results: 1-4 |
Results: 4

Authors: Beltcheva, O Martin, P Lenkkeri, U Tryggvason, K
Citation: O. Beltcheva et al., Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome, HUM MUTAT, 17(5), 2001, pp. 368-373

Authors: Patrakka, J Kestila, M Wartiovaara, J Ruotsalainen, V Tissari, P Lenkkeri, U Mannikko, M Visapaa, I Holmberg, C Rapola, J Tryggvason, K Jalanko, H
Citation: J. Patrakka et al., Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients, KIDNEY INT, 58(3), 2000, pp. 972-980

Authors: Ruotsalainen, V Ljungberg, P Wartiovaara, J Lenkkeri, U Kestila, M Jalanko, H Holmberg, C Tryggvason, K
Citation: V. Ruotsalainen et al., Nephrin is specifically located at the slit diaphragm of glomerular podocytes, P NAS US, 96(14), 1999, pp. 7962-7967

Authors: Lenkkeri, U Mannikko, M McCready, P Lamerdin, J Gribouval, O Niaudet, P Antignac, C Kashtan, CE Holmberg, C Olsen, A Kestila, M Tryggvason, K
Citation: U. Lenkkeri et al., Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations, AM J HU GEN, 64(1), 1999, pp. 51-61
Risultati: 1-4 |