Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis.

Advances in nephrology from the Necker Hospital

Volumn 27, Issue , 1997, Pages 343-359

  Simon, D B ^a   Lifton, R P ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; ION;

ALKALOSIS; BARTTER SYNDROME; GENETICS; HUMAN; HYPOKALEMIA; KIDNEY; METABOLISM; MUTATION; REVIEW; SYNDROME;

ALKALOSIS; BARTTER SYNDROME; CARRIER PROTEINS; HUMANS; HYPOKALEMIA; IONS; KIDNEY; MUTATION; SYNDROME;

EID: 0031304040     PISSN: 00845957     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (39)