Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-13620-9.pdf
Reference45 articles.
1. Dror, A. A. & Avraham, K. B. Hearing loss: mechanisms revealed by genetics and cell biology. Annu Rev Genet 43, 411–37 (2009).
2. Petit, C. Usher syndrome: from genetics to pathogenesis. Annu Rev Genomics Hum Genet 2, 271–97 (2001).
3. Pakarinen, L., Karjalainen, S., Simola, K. O., Laippala, P. & Kaitalo, H. Usher’s syndrome type 3 in Finland. Laryngoscope 105, 613–7 (1995).
4. Ness, S. L. et al. Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III. J Med Genet 40, 767–72 (2003).
5. Plantinga, R. F. et al. Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients. Audiol Neurootol 10, 79–89 (2005).
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