Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function

Biochemical and Biophysical Research Communications

Volumn 230, Issue 3, 1997, Pages 641-645

  Derst, Christian ^a   Konrad, Martin ^a   Köckerling, Arnold ^a   Károlyi, Lothar ^a   Deschenes, Georges ^b   Daut, Jürgen ^a   Karschin, Andreas ^c   Seyberth, Hannsjörg W ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b ARMAND TROUSSEAU HOSPITAL   (France)

^c MAX PLANCK INSTITUTE FOR BIOPHYSICAL CHEMISTRY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BARIUM ION; MAGNESIUM ION; MUTANT PROTEIN; POTASSIUM CHANNEL;

APICAL MEMBRANE; ARTICLE; BARTTER SYNDROME; CELL MEMBRANE POTENTIAL; CLINICAL ARTICLE; ELECTROPHYSIOLOGY; FEMALE; GENE MUTATION; GENETIC TRANSFECTION; GESTATIONAL AGE; HENLE LOOP; HUMAN; HUMAN CELL; KIDNEY CELL; MALE; PATCH CLAMP; POTASSIUM CURRENT; PRENATAL PERIOD; PRIORITY JOURNAL; SALT LOSING NEPHRITIS;

ACACIA SEYAL;

EID: 0031584084     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1996.6024     Document Type: Article

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