Characterization of a novel enu-generated myosin vi mutant mouse strain with congenital deafness and vestibular dysfunction

Hearing Research

Volumn 299, Issue , 2013, Pages 53-62

  Williams, Louise H ^a   Miller, Kerry A ^a   Dahl, Hans Henrik M ^a,b   Manji, Shehnaaz S M ^a,b  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ETHYLNITROSOUREA; MYOSIN VI;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL STRUCTURE; CONGENITAL DEAFNESS; CONTROLLED STUDY; EXON SKIPPING; GENE MUTATION; HAIR CELL; IMMUNOHISTOCHEMISTRY; MOUSE; MOUSE MUTANT; MYO6 GENE; NERVE DEGENERATION; NEUROEPITHELIUM; NONHUMAN; PERINATAL PERIOD; PRIORITY JOURNAL; SCANNING ELECTRON MICROSCOPY; VESTIBULAR DISORDER;

AMINO ACID SEQUENCE; ANIMALS; AUDITORY PERCEPTION; BASE SEQUENCE; CARDIOMYOPATHY, HYPERTROPHIC; COCHLEA; DEAFNESS; DISEASE MODELS, ANIMAL; ETHYLNITROSOUREA; GENETIC PREDISPOSITION TO DISEASE; HEARING TESTS; HOMOZYGOTE; IMMUNOHISTOCHEMISTRY; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MICROSCOPY, ELECTRON, SCANNING; MOLECULAR SEQUENCE DATA; MUTAGENS; MUTATION; MYOSIN HEAVY CHAINS; PHENOTYPE; VESTIBULE, LABYRINTH;

EID: 84876460957     PISSN: 03785955     EISSN: 18785891     Source Type: Journal    
DOI: 10.1016/j.heares.2013.02.006     Document Type: Article

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