Ion transporter mutations in Gitelman's and Bartter's syndromes

Current Opinion in Nephrology and Hypertension

Volumn 7, Issue 1, 1998, Pages 43-47

  Simon, David B ^a,b   Lifton, Richard P ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BARTTER SYNDROME; BLOOD PRESSURE REGULATION; CLINICAL FEATURE; GENE MUTATION; GENETIC ANALYSIS; GITELMAN SYNDROME; HUMAN; HYPOKALEMIC ALKALOSIS; HYPOTENSION; ION TRANSPORT; PATHOPHYSIOLOGY; PRIORITY JOURNAL; REVIEW; SALT LOSING NEPHRITIS;

ALKALOSIS; ANIMALS; BARTTER SYNDROME; CARRIER PROTEINS; HUMANS; HYPOTENSION; MUTATION; SYNDROME;

EID: 0031974389     PISSN: 10624821     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041552-199801000-00008     Document Type: Review

References (28)

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