Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference6 articles.
1. Shearer AE, Hildebrand MS, Smith RJH. Hereditary hearing loss and deafness overview. In: GeneReviews®. 1999. https://www.ncbi.nlm.nih.gov/books/NBK1434/.
2. 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.
3. Rost S, Bach E, Neuner C, Nanda I, Dysek S, Bittner RE, et al. Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6. Eur J Hum Genet. 2014;22:208–15.
4. 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.
5. 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.
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1. New year, new issue;European Journal of Human Genetics;2021-12-01