A novel MYH9 mutation related to non-syndromic delayed post-lingual sensorineural hearing loss
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Otorhinolaryngology
Link
https://link.springer.com/content/pdf/10.1007/s00405-021-06976-2.pdf
Reference17 articles.
1. Dror AA, Avraham KB (2009) Hearing loss: mechanisms revealed by genetics and cell biology. Annu Rev Genet 43:411–437
2. Alford RL, Arnos KS, Fox M, Lin JW, Palmer CG, Pandya A et al (2014) American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. Genet Med 16:347–355
3. Chang KW (2015) Genetics of hearing loss-nonsyndromic. Otolaryngol Clin North Am 48:1063–1072
4. Lenz DR, Avraham KB (2011) Hereditary hearing loss: from human mutation to mechanism. Hear Res 281:3–10
5. Pecci A, Ma X, Savoia A, Adelstein RS (2018) MYH9: structure, functions and role of non-muscle myosin IIA in human disease. Gene 20:152–167
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