Journal article

An ENU-Induced Mutation of Cdh23 Causes Congenital Hearing Loss, but No Vestibular Dysfunction, in Mice

Shehnaaz SM Manji, Kerry A Miller, Louise H Williams, Lotte Andreasen, Maria Siboe, Elizabeth Rose, Melanie Bahlo, Michael Kuiper, Hans-Henrik M Dahl

American Journal of Pathology | ELSEVIER SCIENCE INC | Published : 2011

DOI: 10.1016/j.ajpath.2011.04.002

Grants

Awarded by National Health and Medical Research Council

Funding Acknowledgements

Supported by grant 436944 from the National Health and Medical Research Council, the HEARing CRC, and J. & J. Calvert-Jones.

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Keywords

Science & Technology
Humans
Vestibule, Labyrinth
Hearing
Cadherin Gene
Cadherins
Syndrome Type 1d
Mutation
Nonsyndromic Deafness
Waltzer Mice
Pathology
Molecular-Dynamics
Ethylnitrosourea
Sequence Homology, Amino Acid
Dna Mutational Analysis
Mouse Model
Usher-Syndrome
Mechanosensory Hair-Cells
Functional Interaction
Models, Molecular
Protein Conformation
Molecular Sequence Data
Hearing Loss, Sensorineural
Mice
Mice, Transgenic
Tip-Link
Life Sciences & Biomedicine
Alleles
Amino Acid Sequence
Vestibular Diseases
Animals