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