Genetic disorders of transporters/channels in the inner ear and their relation to the kidney

Pediatric Nephrology

Volumn 19, Issue 11, 2004, Pages 1194-1201

  Peters, Theo A ^a   Monnens, Leo A H ^a   Cremers, Cor W R J ^a   Curfs, Jo H A J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Deafness; Endolymph; Hereditary; Inner ear; Transport disorders

Indexed keywords

AQUAPORIN 4; BICARBONATE SODIUM COTRANSPORTER; CHLORIDE CHANNEL; CHLORIDE ION; POTASSIUM CHANNEL KCNQ1; POTASSIUM ION; PROTON PUMP; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATASE; SERINE PROTEINASE; SODIUM CHANNEL; SODIUM ION; SODIUM POTASSIUM CHLORIDE COTRANSPORTER; SODIUM PROTON EXCHANGE PROTEIN 3;

BARTTER SYNDROME; CHLORIDE TRANSPORT; COCHLEA; DISEASE ASSOCIATION; ENDOLYMPH AND PERILYMPH; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; HEARING IMPAIRMENT; HUMAN; INNER EAR DISEASE; KIDNEY DISEASE; KIDNEY TUBULE ACIDOSIS; LONG QT SYNDROME; MOUSE; NONHUMAN; PATHOLOGICAL ANATOMY; PENDRED SYNDROME; POTASSIUM TRANSPORT; PRIORITY JOURNAL; PROTON SODIUM EXCHANGE; REVIEW; SODIUM TRANSPORT;

ANIMALS; CHILD; EAR, INNER; HEARING LOSS, SENSORINEURAL; HUMANS; KIDNEY DISEASES; LABYRINTH DISEASES; MEMBRANE TRANSPORT PROTEINS; MICE; MODELS, ANIMAL;

EID: 7944224833     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-004-1626-6     Document Type: Review

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