New year, new issue
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-021-01014-5.pdf
Reference15 articles.
1. Bharadwaj T, Schrauwen I, Rehman S, Liaqat K, Acharya A, Giese APJ, et al. ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00913-x
2. Bueno AS, Nunes K, Dias AMM, Alves LU, Mendes BCA, Sampaio-Silva J, et al. Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00891-0
3. O’Brien A, Aw WY, Tee HY, Naegeli KM, Bademci G, Tekin M, et al. Confirmation of COL4A6 variants in X-linked nonsyndromic hearing loss and its clinical implications. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00881-2
4. Vaché C, Baux D, Bianchi J, Baudoin C, Faugère V, Francannet C, et al. Reclassification of a TMC1 synonymous substitution as a variant disrupting splicing regulatory elements associated with recessive hearing loss. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-01010-9
5. Roux A-F. Deafness–family matters. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-01006-5
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