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Results: 1-3 |
Results: 3
Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients
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
Targeted inactivation of the type VII collagen gene (Col7a1) in mice results in severe blistering phenotype: a model for recessive dystrophic epidermolysis bullosa
Authors: Heinonen, S Mannikko, M Klement, JF Whitaker-Menezes, D Murphy, GF Uitto, J
Citation: S. Heinonen et al., Targeted inactivation of the type VII collagen gene (Col7a1) in mice results in severe blistering phenotype: a model for recessive dystrophic epidermolysis bullosa, J CELL SCI, 112(21), 1999, pp. 3641-3648
Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations
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: 1-3 |