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Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.

Myosin VIIa is a newly identified member of the myosin superfamily of actin-based motors. Recently, the myosin VIIa gene was identified as the gene defective in shaker-1, a recessive deafness in mice [Gibson, F., Walsh, J., Mburu, P., Varela, A., Brown, K.A., Antonio, M., Beisel, K.W., Steel, K.P. &...

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Bibliografske podrobnosti
izdano v:Proc Natl Acad Sci U S A
Principais autores: Hasson, T, Heintzelman, M B, Santos-Sacchi, J, Corey, D P, Mooseker, M S
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 1995
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC40893/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7568224/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.92.21.9815
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