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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.
- Published in:
- Human Genetics, 2022, v. 141, n. 3/4, p. 697, doi. 10.1007/s00439-021-02405-w
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- Article