Urbizu, J M <br/><br/>
[Molecular genetic changes identified in tubular disorders affecting water-electrolyte transport].  [electronic resource] 

 -  Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia   
 - 127-36 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>0211-6995 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anion Transport Proteins<br/>Antiporters--genetics<br/>Aquaporin 2<br/>Aquaporin 6<br/>Aquaporins--deficiency<br/>Carrier Proteins--genetics<br/>Chloride Channels--deficiency<br/>Chloride-Bicarbonate Antiporters<br/>Chromosome Mapping<br/>Chromosomes, Human--genetics<br/>Epithelial Sodium Channels<br/>Humans<br/>Ion Transport--genetics<br/>Kidney Tubules--metabolism<br/>Kidney Tubules, Proximal--metabolism<br/>Loop of Henle--metabolism<br/>Membrane Proteins<br/>Potassium Channels--deficiency<br/>Potassium Channels, Inwardly Rectifying<br/>Proton-Translocating ATPases--deficiency<br/>Renal Tubular Transport, Inborn Errors--genetics<br/>Sodium Channels--deficiency<br/>Sodium Chloride Symporters<br/>Sodium-Bicarbonate Symporters<br/>Sodium-Potassium-Chloride Symporters<br/>Symporters<br/>Water-Electrolyte Imbalance--genetics