Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

Pediatric Research

Volumn 48, Issue 6, 2000, Pages 754-758

  Jeck, Nikola ^a   Konrad, Martin ^a   Peters, Melanie ^a   Weber, Stefanie ^a   Bonzel, Klaus E ^b   Seyberth, Hannsjörg W ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BARTTER SYNDROME; CASE REPORT; CHILD; DEHYDRATION; ELECTROLYTE DISTURBANCE; ENDOPLASMIC RETICULUM; GENE MUTATION; GENETIC HETEROGENEITY; GITELMAN SYNDROME; HUMAN; HYPOCALCIURIA; HYPOKALEMIA; HYPOKALEMIC ALKALOSIS; PHENOTYPE; PRIORITY JOURNAL; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM;

EID: 0033667558     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-200012000-00009     Document Type: Article

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