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Editorial
. 2020 Nov;13(4):315-317.
doi: 10.21053/ceo.2020.01606. Epub 2020 Nov 1.

Genetic Information and Precision Medicine in Hearing Loss

Doo-Yi Oh  1 , Byung Yoon Choi  1
Affiliations
Editorial

Genetic Information and Precision Medicine in Hearing Loss

Doo-Yi Oh et al. Clin Exp Otorhinolaryngol. 2020 Nov.
No abstract available

PubMed Disclaimer

Conflict of interest statement

No potential conflict of interest relevant to this article was reported.

References

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    1. Kim NK, Kim AR, Park KT, Kim SY, Kim MY, Nam JY, et al. Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population. Genet Med. 2015 Nov;17(11):901–11. - PubMed
    1. Kim BJ, Oh DY, Han JH, Oh J, Kim MY, Park HR, et al. Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach. Genet Med. 2020 Jun;22(6):1119–28. - PubMed
    1. Yu Y, Yang Y, Lu J, Jin Y, Yang Y, Hong E, et al. Two compound heterozygous were identified in SLC26A4 gene in two Chinese families with enlarged vestibular aqueduct. Clin Exp Otorhinolaryngol. 2019 Feb;12(1):50–7. - PMC - PubMed

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