Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

Human Molecular Genetics

Volumn 10, Issue 2, 2001, Pages 153-161

  Everett, Lorraine A ^a   Belyantseva, Inna A ^b   Noben Trauth, Konrad ^b   Cantos, Raquel ^b   Chen, Amy ^a   Thakkar, Sneha I ^a   Hoogstraten Miller, Shelley L ^a   Kachar, Bechara ^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

CARRIER PROTEIN; PENDRIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONFOCAL MICROSCOPY; CONTROLLED STUDY; EAR MALFORMATION; EMBRYO DEVELOPMENT; ENDOLYMPH; FLUORESCENCE MICROSCOPY; GENE DISRUPTION; GENE MUTATION; GENE TARGETING; HEARING IMPAIRMENT; INNER EAR DISEASE; KNOCKOUT MOUSE; MOUSE; NERVE CELL DEGENERATION; NONHUMAN; OTOLITH; PATHOGENESIS; PENDRED SYNDROME; PERINATAL PERIOD; PRIORITY JOURNAL; SCANNING ELECTRON MICROSCOPY; SENSORY NERVE CELL; VESTIBULAR DISORDER; VESTIBULE;

EID: 0035862723     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.2.153     Document Type: Article

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