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Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 21, p. 13453, doi. 10.3390/ijms232113453
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- Article
Updated carrier rates for c.35delG ( GJB2 ) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
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- BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0650-5
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- Article
Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia).
- Published in:
- Genes, 2023, v. 14, n. 4, p. 928, doi. 10.3390/genes14040928
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- Article
High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect.
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- Genes, 2020, v. 11, n. 7, p. 833, doi. 10.3390/genes11070833
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- Article
Different Rates of the SLC26A4 -Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).
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- Diagnostics (2075-4418), 2021, v. 11, n. 12, p. 2378, doi. 10.3390/diagnostics11122378
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- Article
Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains.
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- Biomolecules (2218-273X), 2023, v. 13, n. 10, p. 1521, doi. 10.3390/biom13101521
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- Article