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. 2001:31:55-68.

Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families

S Disse-Nicodème, J M Achard, J Potier, M Delahousse, B Fiquet-Kempf, N Stern, A Blanchard, J C Guilbaud, P Niaudet, D Chauveau, B Dussol, Y Berland, P Dequiedt, J L Ader, M Paillard, J P Grünfeld, A Fournier, P Corvol, X Jeunemaitre
  • PMID: 11692471

Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families

S Disse-Nicodème et al. Adv Nephrol Necker Hosp. 2001.
No abstract available

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