Authors:
Konrad, M
Vollmer, M
Lemmink, HH
Van den Heuvel, LPWJ
Jeck, N
Vargas-Poussou, R
Lakings, A
Ruf, R
Deschenes, G
Antignac, C
Guay-Woodford, L
Knoers, NVAM
Seyberth, HW
Feldmann, D
Hildebrandt, F
Citation: M. Konrad et al., Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome, J AM S NEPH, 11(8), 2000, pp. 1449-1459
Authors:
Kunzelmann, K
Hubner, M
Vollmer, M
Ruf, R
Hildebrandt, F
Greger, R
Schreiber, R
Citation: K. Kunzelmann et al., A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects onK+ conductance, CELL PHYS B, 10(3), 2000, pp. 117-124
Authors:
Vollmer, M
Kremer, M
Ruf, R
Miot, S
Nothwang, HG
Wirth, J
Otto, E
Krapf, R
Hildebrandt, F
Citation: M. Vollmer et al., Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes, GENOMICS, 68(2), 2000, pp. 127-135
Authors:
Vollmer, M
Jung, M
Ruschendorf, F
Ruf, R
Wienker, T
Reis, A
Krapf, R
Hildebrandt, F
Citation: M. Vollmer et al., The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster, AM J HU GEN, 63(6), 1998, pp. 1724-1731