Disorders of the epithelial Na+ channel in Liddle's syndrome and autosomal recessive pseudohypoaldosteronism type 1

Experimental Nephrology

Volumn 8, Issue 6, 2000, Pages 320-325

  Young S, Oh ^a   Warnock, David G ^b  

^a University of Alabama at Birmingham   (United States)

^b University of Alabama at Birmingham   (United States)

Author keywords

Epithelial Na+ channel; Genetic defects; Hypertension; Pathophysiology

Indexed keywords

ALDOSTERONE; CARRIER PROTEIN; SODIUM ION;

AUTOSOMAL RECESSIVE DISORDER; DISEASE ASSOCIATION; GENE MUTATION; GENETIC LINKAGE; HUMAN; LIDDLE SYNDROME; MOLECULAR CLONING; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PSEUDOHYPOALDOSTERONISM; REVIEW; SODIUM CHANNEL; SODIUM CURRENT;

ANIMAL; GENES, RECESSIVE; HUMAN; HYPERTENSION; PSEUDOHYPOALDOSTERONISM; SODIUM CHANNELS; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0343878252     PISSN: 10187782     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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