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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:
Park, JH
Dixit, MP
Onuchic, LF
Wu, GQ
Goncharuk, AN
Kneitz, S
Santarina, LB
Hayashi, T
Avner, ED
Guay-Woodford, L
Zerres, K
Germino, GG
Somlo, S
Citation: Jh. Park et al., A 1-Mb BAC/PAC-Based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6, GENOMICS, 57(2), 1999, pp. 249-255
Citation: Pd. Wilson et L. Guay-woodford, Pathophysiology and clinical management of polycystic kidney disease in women, SEM NEPHROL, 19(2), 1999, pp. 123-132