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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss.
J Hum Genet. 2023 Oct;68(10):657-669. doi: 10.1038/s10038-023-01159-9. Epub 2023 May 22.
J Hum Genet. 2023.
PMID: 37217689
Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population.
Figueroa-Ildefonso E, Bademci G, Rajabli F, Cornejo-Olivas M, Villanueva RDC, Badillo-Carrillo R, Inca-Martinez M, Neyra KM, Sineni C, Tekin M.
Figueroa-Ildefonso E, et al.
Genes (Basel). 2019 Jul 31;10(8):581. doi: 10.3390/genes10080581.
Genes (Basel). 2019.
PMID: 31370293
Free PMC article.
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