Author:
Bailey M.A.,Cantone A.,Yan Q.,MacGregor G.G.,Leng Q.,Amorim J.B.O.,Wang T.,Hebert S.C.,Giebisch G.,Malnic G.
Reference60 articles.
1. Bartter syndrome;Hebert;Curr Opin Nephrol Hypertens,2003
2. Pharmacotyping of hypokalaemic salt-losing tubular disorders;Reinalter;Acta Physiol Scand,2004
3. Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity;Karolyil;Hum Mol Genet,1997
4. Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK;Simon;Nat Genet,1996
5. Microperfusion study of distal tubular potassium and sodium transfer in rat kidney;Malnic;Am J Physiol,1966
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