Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear

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

Volumn 96, Issue 17, 1999, Pages 9727-9732

  Everett, Lorraine A ^a   Morsli, Hakim ^b   Wu, Doris K ^b   Green, Eric D ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; ENDOLYMPH; GENE EXPRESSION; GENE ISOLATION; HEARING IMPAIRMENT; INNER EAR; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PENDRED SYNDROME; PRIORITY JOURNAL; SACCULUS; UTRICLE; VESTIBULE AQUEDUCT;

AMINO ACID SEQUENCE; ANIMALS; BIOLOGICAL TRANSPORT; CARRIER PROTEINS; COCHLEA; DEAFNESS; DNA; EAR, INNER; GENE EXPRESSION REGULATION; GOITER; HUMANS; IN SITU HYBRIDIZATION; MEMBRANE TRANSPORT PROTEINS; MICE; MOLECULAR SEQUENCE DATA; RATS; SEQUENCE ALIGNMENT; SYNDROME;

EID: 0033578352     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.17.9727     Document Type: Article

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