Deafness-family matters
- PMID: 34819629
- PMCID: PMC8738762
- DOI: 10.1038/s41431-021-01006-5
Deafness-family matters
Conflict of interest statement
The author declares no competing interests.
Comment on
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Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletions.Eur J Hum Genet. 2021 Aug;29(8):1292-1300. doi: 10.1038/s41431-021-00856-3. Epub 2021 Mar 22. Eur J Hum Genet. 2021. PMID: 33753912 Free PMC article.
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Confirmation of COL4A6 variants in X-linked nonsyndromic hearing loss and its clinical implications.Eur J Hum Genet. 2022 Jan;30(1):7-12. doi: 10.1038/s41431-021-00881-2. Epub 2021 Apr 12. Eur J Hum Genet. 2022. PMID: 33840813 Free PMC article.
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Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss.Eur J Hum Genet. 2022 Jan;30(1):13-21. doi: 10.1038/s41431-021-00891-0. Epub 2021 May 6. Eur J Hum Genet. 2022. PMID: 33953343 Free PMC article.
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ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment.Eur J Hum Genet. 2022 Jan;30(1):22-33. doi: 10.1038/s41431-021-00913-x. Epub 2021 Jun 16. Eur J Hum Genet. 2022. PMID: 34135477 Free PMC article.
References
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- Shearer AE, Hildebrand MS, Smith RJH. Hereditary hearing loss and deafness overview. In: GeneReviews®. 1999. https://www.ncbi.nlm.nih.gov/books/NBK1434/.
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