Hereditary hearing loss; about the known and the unknown
Author:
Publisher
Elsevier BV
Subject
Sensory Systems
Reference145 articles.
1. Prevalence of hearing loss and differences by demographic characteristics among US adults: data from the National Health and Nutrition Examination Survey, 1999-2004;Agrawal;Arch. Intern. Med.,2008
2. A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family;Behlouli;Int. J. Pediatr. Otorhinolaryngol.,2016
3. Organization and function of the 3D genome;Bonev;Nat. Rev. Genet.,2016
4. An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients;Bonnet;Eur. J. Hum. Genet.,2016
5. Intracellular regulome variability along the organ of corti: evidence, approaches, challenges, and perspective;Booth;Front. Genet.,2018
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