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) › Research Explorer

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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)

Research output: Contribution to journal › Article › peer-review

DOI

https://doi.org/10.3390/genes14040928
Final published version

Original language	English
Article number	928
Journal	Genes
Volume	14
Issue number	4
DOIs	https://doi.org/10.3390/genes14040928
Publication status	Published - 17 Apr 2023

OECD FOS+WOS

3.02 CLINICAL MEDICINE
1.06 BIOLOGICAL SCIENCES

Research areas

Humans, Siberia/epidemiology, Mutation, Hearing Loss/genetics, Deafness/genetics, Russia, Sulfate Transporters/genetics

ID: 49071377