Multiple Mutations of MYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss

Myosin I isozymes have been implicated in various motile processes, including organelle translocation, ion-channel gating, and cytoskeleton reorganization. Unconventional myosins were among the first family of proteins found to be associated with hearing loss in both humans and mice. Here, we report...

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Hlavní autoři: Donaudy, Francesca, Ferrara, Antonella, Esposito, Laura, Hertzano, Ronna, Ben-David, Orit, Bell, Rachel E., Melchionda, Salvatore, Zelante, Leopoldo, Avraham, Karen B., Gasparini, Paolo
Médium: Artigo
Jazyk:Inglês
Vydáno: The American Society of Human Genetics 2003
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1180318/
https://ncbi.nlm.nih.gov/pubmed/12736868
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