go back to reference International Collaborative Study Group for Bartter-like Syndromes, consisting of: Group 1: Károlyi L, Konrad M, Köckerling A, Ziegler A, Zimmermann DK, Roth B, Wieg C, Grzeschik K-H, Koch MC, Seyberth HW, Group 2: Vargas R, Forestier L, Jean G, Deschaux M, Rizzoni GF, Niaudet P, Antignac C, Group 3: Feldmann D, Lorridon F, Cougoureux E, Laroze F, Alessandri J-L, David L, Saunier P, Deschenes G, Group 4: Hildebrandt F, Vollmer M, Proesmans W, Brandis M, Group 5: van den Heuvel LP, Lemmink HH, Nillesen W, Monnens LAH, Knoers NVAM, Group 6: Guay-Woodford LM, Wright CJ, Madrigal G and Hebert SC (1997) Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity. Hum Mol Genet 6:17–26CrossRef
International Collaborative Study Group for Bartter-like Syndromes, consisting of:
Group 1: Károlyi L, Konrad M, Köckerling A, Ziegler A, Zimmermann DK, Roth B, Wieg C, Grzeschik K-H, Koch MC, Seyberth HW,
Group 2: Vargas R, Forestier L, Jean G, Deschaux M, Rizzoni GF, Niaudet P, Antignac C,
Group 3: Feldmann D, Lorridon F, Cougoureux E, Laroze F, Alessandri J-L, David L, Saunier P, Deschenes G,
Group 4: Hildebrandt F, Vollmer M, Proesmans W, Brandis M,
Group 5: van den Heuvel LP, Lemmink HH, Nillesen W, Monnens LAH, Knoers NVAM,
Group 6: Guay-Woodford LM, Wright CJ, Madrigal G and Hebert SC (1997) Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity. Hum Mol Genet 6:17–26
CrossRef