A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA

The motor protein myosin IIIA is critical for maintenance of normal hearing. Homozygosity and compound heterozygosity for loss-of-function mutations in MYO3A, which encodes myosin IIIA, are responsible for inherited human progressive hearing loss DFNB30. To further evaluate this hearing loss, we con...

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Detalhes bibliográficos
Publicado no:Mamm Genome
Main Authors: Walsh, Vanessa L., Raviv, Dorith, Dror, Amiel A., Shahin, Hashem, Walsh, Tom, Kanaan, Moien N., Avraham, Karen B., King, Mary-Claire
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8023428/
https://ncbi.nlm.nih.gov/pubmed/21165622
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-010-9310-6
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