The diagnosis of Liddle syndrome by identification of a mutation in the beta subunit of the epithelial sodium channel.

Author:

Jackson S N,Williams B,Houtman P,Trembath R C

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. Molecular genetics of human blood pressure regulation;Lifton, R.P.;Science,1996

2. A familial renal disorder simulating primary aldosteronism but with negligible aldosterone secretion;Liddle, G.W.; Bledsoe, T.; WS, Jr, Coppage;Trans Assoc Am Phys,1963

3. Arginine vasopressin and forskolin regulate apical cell surface expression of epithelial Na+ channels in A6 cells;Kleyman, T.R.; Ernst, S.A.; Coupaye-Gerard, B.;Am J Physiol,1994

4. et aL Mechanisms by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel;Snyder, P.M.; Price, M.P.; McDonald, F.J.;Cell,1995

5. A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol;Ulick, S.; Levine, L.S.; Gunczler, P.;Jf Clin Endocrinol Metab,1979

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