Noggin heterozygous mice: An animal model for congenital conductive hearing loss in humans

Human Molecular Genetics

Volumn 17, Issue 6, 2008, Pages 844-853

  Hwang, Chan Ho ^a   Wu, Doris K ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN 4; GROWTH DIFFERENTIATION FACTOR 5; NOGGIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDITORY OSSICLE; AUDITORY THRESHOLD; AUTOSOMAL DOMINANT DISORDER; CARTILAGE CELL; CELL HYPERPLASIA; CONDUCTION DEAFNESS; CONTROLLED STUDY; EARDRUM; ECTOPIC TISSUE; EMBRYO; GENE MUTATION; HETEROZYGOSITY; MOUSE; NONHUMAN; OSSIFICATION; PERCEPTION DEAFNESS; PRIORITY JOURNAL; STAPES;

ANIMALS; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; DISEASE MODELS, ANIMAL; HEARING LOSS, CONDUCTIVE; HETEROZYGOTE; HUMANS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; SENSORY THRESHOLDS;

ANIMALIA; MUS;

EID: 40549126625     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddm356     Document Type: Article

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