Genetics of deafness
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference61 articles.
1. Genes and deafness;Steel;Trends Genet,1994
2. Inherited hearing defects in mice;Steel;Annu Rev Genet,1995
3. A type VII myosin encoded by the mouse deafness gene shaker-1;Gibson;Nature,1995
4. Defective myosin VIIA gene responsible for Usher syndrome type 1B;Weil;Nature,1995
5. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells;Avraham;Nature Genet,1995
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1. Phenotypic differences in the inner ears of CBA/CaJ and C57BL/6J mice carrying missense and single base pair deletion mutations in the Cdh23 gene;Journal of Neuroscience Research;2021-06-16
2. Basilar Membrane and Tectorial Membrane Stiffness in the CBA/CaJ Mouse;Journal of the Association for Research in Otolaryngology;2014-05-28
3. A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss;PLoS ONE;2014-02-21
4. Cochlear Implant Considerations in Children with Additional Disabilities;Current Otorhinolaryngology Reports;2013-02-01
5. Cognitive Outcomes and Familial Stress After Cochlear Implantation in Deaf Children With and Without Developmental Delays;Otology & Neurotology;2012-08
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