Hearing loss in the laminin-deficient dy mouse model of congenital muscular dystrophy

Molecular Genetics and Metabolism

Volumn 76, Issue 3, 2002, Pages 217-224

  Pillers, De Ann M ^a   Kempton, J Beth ^b   Duncan, Nancy M ^a   Pang, Jiaqing ^a   Dwinnell, Shannon J ^a   Trune, Dennis R ^b  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

Animal model; Auditory brainstem response; Cochlea; DFNA10; Laminin; Mouse; Muscular dystrophy; Sensorineural hearing loss

Indexed keywords

MEROSIN;

ANATOMY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDITORY RESPONSE; AUDITORY STIMULATION; AUDITORY THRESHOLD; BRAIN STEM RESPONSE; CELL INFILTRATION; COCHLEA; CONNECTIVE TISSUE; CONTROLLED STUDY; CORTI ORGAN; DISEASE ASSOCIATION; DISEASE MODEL; EAR; EVALUATION; FEMALE; HEARING LOSS; HOMOZYGOSITY; INNER EAR DISEASE; LAMININ DEFICIENCY; MOUSE; MUSCULAR DYSTROPHY; NONHUMAN; PATHOLOGY; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN FUNCTION; PURE TONE AUDIOMETRY; RADIOFREQUENCY;

ANIMALS; BRAIN STEM; DISEASE MODELS, ANIMAL; EAR, INNER; HEARING LOSS, SENSORINEURAL; LAMININ; MICE; MICE, INBRED C57BL; MUSCULAR DYSTROPHIES;

ANIMALIA;

EID: 0036375020     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1096-7192(02)00039-2     Document Type: Article

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