Myosin Mutations and Sudden Sensorineural Hearing Loss: Results of Whole Exome Sequencing

Sharma, R. K., Drusin, M., Hostyk, J., Baugh, E. H., Aggarwal, V. S., Goldstein, D., & Kim, A. H. (2022). Myosin Mutations and Sudden Sensorineural Hearing Loss: Results of Whole Exome Sequencing. Otology & Neurotology, 44(1), 16–20. https://doi.org/10.1097/mao.0000000000003756
Authors:
Rahul K Sharma
Madeleine Drusin
Joseph Hostyk
Evan H Baugh
Vimla S Aggarwal
David Goldstein
Ana H Kim
Affiliated Authors:
Madeleine Drusin
Ana H Kim
Columbia Affiliation:
Subjects:
Hearing Loss, Sudden (MeSH)
Hearing Loss, Sensorineural (MeSH)
Deafness (MeSH)
Author Keywords:
genetics
myosin
sudden sensorineural hearing loss
whole-exome sequencing
elink
Publication Type:
Article
Unique ID:
10.1097/mao.0000000000003756
PMID:
36509433
DOI:
10.1097/mao.0000000000003756
Journal:
Otology and Neurotology
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record
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Record Created: