Auditory phenotype of DFNA17
- PMID: 12408071
- DOI: 10.1159/000066818
Auditory phenotype of DFNA17
Similar articles
-
R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17.Clin Genet. 2015 Jul;88(1):85-9. doi: 10.1111/cge.12438. Epub 2014 Jul 26. Clin Genet. 2015. PMID: 24890873
-
Cochlear implants for DFNA17 deafness.Laryngoscope. 2006 Dec;116(12):2211-5. doi: 10.1097/01.mlg.0000242089.72880.f8. Laryngoscope. 2006. PMID: 17146397
-
Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis.Hear Res. 2013 May;299:88-98. doi: 10.1016/j.heares.2012.12.015. Epub 2013 Jan 20. Hear Res. 2013. PMID: 23340379
-
Clinical presentation of the DFNA loci where causative genes have not yet been cloned. DFNA4, DFNA6/14, DFNA7, DFNA16, DFNA20 and DFNA21.Adv Otorhinolaryngol. 2002;61:98-106. doi: 10.1159/000066820. Adv Otorhinolaryngol. 2002. PMID: 12408070 Review. No abstract available.
-
[Otoacoustic emissions, auditory evoked potentials, pure tone thresholds and speech intelligibility in cases of auditory neuropathy].HNO. 2000 Jan;48(1):28-32. doi: 10.1007/s001060050005. HNO. 2000. PMID: 10663046 Review. German.
Cited by
-
Generation and characterization of mice with Myh9 deficiency.Neuromolecular Med. 2007;9(3):205-15. doi: 10.1007/s12017-007-8008-8. Neuromolecular Med. 2007. PMID: 17914179
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous