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Results: 3

Authors: Wilson, FH Disse-Nicodeme, S Choate, KA Ishikawa, K Nelson-Willams, C Desitter, I Gunel, M Milford, DV Lipkin, GW Achard, JM Feely, MP Dussol, B Berland, Y Unwin, RJ Mayan, H Simon, DB Farfel, Z Jeunemaitre, X Lifton, RP
Citation: Fh. Wilson et al., Human hypertension caused by mutations in WNK kinases, SCIENCE, 293(5532), 2001, pp. 1107-1112

Authors: Smith, AN Skaug, J Choate, KA Nayir, A Bakkaloglu, A Ozen, S Hulton, SA Sanjad, SA Al-Sabban, EA Lifton, RP Scherer, SW Karet, FE
Citation: An. Smith et al., Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing, NAT GENET, 26(1), 2000, pp. 71-75

Authors: Simon, DB Lu, Y Choate, KA Velazquez, H Al-Sabban, E Praga, M Casari, C Bettinelli, A Colussi, C Rodriguez-Soriano, J McCredie, D Milford, D Sanjad, S Lifton, RP
Citation: Db. Simon et al., Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption, SCIENCE, 285(5424), 1999, pp. 103-106
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