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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 1 |
2023 | 2 |
2024 | 0 |
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3 results
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Page 1
Syntaxin 4 is essential for hearing in human and zebrafish.
Hum Mol Genet. 2023 Mar 20;32(7):1184-1192. doi: 10.1093/hmg/ddac257.
Hum Mol Genet. 2023.
PMID: 36355422
Free PMC article.
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana.
Adadey SM, Aboagye ET, Esoh K, Acharya A, Bharadwaj T, Lin NS, Amenga-Etego L, Awandare GA, Schrauwen I, Leal SM, Wonkam A.
Adadey SM, et al.
BMC Med Genomics. 2022 Nov 10;15(1):237. doi: 10.1186/s12920-022-01391-w.
BMC Med Genomics. 2022.
PMID: 36357908
Free PMC article.
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Nonsense variant in a consanguineous family expands the phenotype of KPTN gene-related syndrome to include hearing impairment.
Liaqat K, Bharadwaj T, Shah K, Nasir A, Acharya A, Khan S, Ullah I, Schrauwen I, Ahmad W, Leal SM.
Liaqat K, et al.
Clin Genet. 2023 Oct;104(4):499-501. doi: 10.1111/cge.14390. Epub 2023 Jun 13.
Clin Genet. 2023.
PMID: 37311648
Free PMC article.
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