KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway

Proceedings of the National Academy of Sciences of the United States of America

Volumn 97, Issue 8, 2000, Pages 4333-4338

  Kharkovets, Tatjana ^a   Hardelin, Jean Pierre ^b   Safieddine, Saaid ^b   Schweizer, Michaela ^a   El Amraoui, Aziz ^b   Petit, Christine ^b   Jentsch, Thomas J ^a  

^a UNIVERSITY OF HAMBURG   (Germany)

^b INSTITUT PASTEUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL;

ANIMAL CELL; ARTICLE; AUDITORY NERVOUS SYSTEM; COCHLEA; COCHLEAR NUCLEUS; GENE EXPRESSION; GENE MUTATION; HAIR CELL; HEARING IMPAIRMENT; HEARING LOSS; INFERIOR COLLICULUS; INNER EAR; MALE; MEMBRANE STEADY POTENTIAL; MOUSE; NONHUMAN; PRIORITY JOURNAL; RAT; SENSORY NERVE CELL;

AMINO ACID SEQUENCE; ANIMALS; AUDITORY PATHWAYS; BRAIN; COS CELLS; EAR, INNER; GENES, DOMINANT; HEARING LOSS, SENSORINEURAL; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; KCNQ POTASSIUM CHANNELS; MICE; MICE, INBRED C3H; MICROSCOPY, ELECTRON; MOLECULAR SEQUENCE DATA; POTASSIUM CHANNELS; POTASSIUM CHANNELS, VOLTAGE-GATED;

ANIMALIA; CALYX; LEMNISCUS;

EID: 0034636056     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.97.8.4333     Document Type: Article

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