Mechanotransduction and Inner Ear Function
Publisher
Springer Singapore
Reference71 articles.
1. Michel, V., et al. 2017. CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival. EMBO Molecular Medicine 9: 1711–1731.
2. Riazuddin, S., et al. 2012. Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nature Genetics 44 (11): 1265–1271.
3. Booth, K.T., et al. 2017. Variants in CIB2 cause DFNB48 and not USH1J. Clinical Genetics. https://doi.org/10.1111/cge.13170 .
4. Bitner-Glindzicz, M., et al. 2000. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene. Nature Genetics 26 (1): 56–60.
5. Verpy, E., et al. 2000. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nature Genetics 26 (1): 51–55.