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A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.
Hum Genet. 2022 Apr;141(3-4):697-707. doi: 10.1007/s00439-021-02405-w. Epub 2021 Nov 27.
Hum Genet. 2022.
PMID: 34839402
Genetic etiology of hearing loss in Russia.
Posukh OL.
Posukh OL.
Hum Genet. 2022 Apr;141(3-4):649-663. doi: 10.1007/s00439-021-02327-7. Epub 2021 Aug 6.
Hum Genet. 2022.
PMID: 34363095
Review.
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