Chronic renal failure in a boy with classic Bartter's syndrome due to a novel mutation in CLCNKB coding for the chloride channel

European Journal of Pediatrics

Volumn 168, Issue 9, 2009, Pages 1129-1133

  Lin, Chien Ming ^a   Tsai, Jeng Daw ^b   Lo, Yi Fen ^a   Yan, Ming Tso ^a   Yang, Sung Sen ^a   Lin, Shih Hua ^a  

^a TRI SERVICE GENERAL HOSPITAL   (Taiwan)

^b MACKAY MEMORIAL HOSPITAL   (Taiwan)

Author keywords

Classic bartter's syndrome; Hypokalemia; NSAIDs; Renal failure

Indexed keywords

CHLORIDE CHANNEL; CLCNKB PROTEIN, HUMAN; SODIUM POTASSIUM CHLORIDE COTRANSPORTER; SODIUM POTASSIUM CHLORIDE COTRANSPORTER 2 PROTEIN; SODIUM-POTASSIUM CHLORIDE COTRANSPORTER 2 PROTEIN;

ADOLESCENT; ARTICLE; CASE REPORT; CHRONIC KIDNEY FAILURE; DISEASE COURSE; GENETICS; HUMAN; HYPOKALEMIA; MALE; MISSENSE MUTATION; POINT MUTATION; SYNDROME;

ADOLESCENT; CHLORIDE CHANNELS; DISEASE PROGRESSION; HUMANS; HYPOKALEMIA; KIDNEY FAILURE, CHRONIC; MALE; MUTATION, MISSENSE; POINT MUTATION; SODIUM-POTASSIUM-CHLORIDE SYMPORTERS; SYNDROME;

EID: 75549086073     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-008-0883-y     Document Type: Article

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