A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia › Research Explorer

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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

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

DOI

https://doi.org/10.1007/s00439-021-02405-w
Final published version

Aisen V. Solovyev
Alena Kushniarevich
Elena Bliznetz
Marita Bady-Khoo
Maria R. Lalayants
Tatiana G. Markova
Gabriel Minárik
L’udevít Kádasi
Ene Metspalu
Vera G. Pshennikova
Fedor M. Teryutin
Elza K. Khusnutdinova
Alexander Poliakov
Mait Metspalu
Olga L. Posukh
Nikolay A. Barashkov
Sardana A. Fedorova

Original language	English
Pages (from-to)	697-707
Number of pages	11
Journal	Human Genetics
Volume	141
Issue number	3-4
DOIs	https://doi.org/10.1007/s00439-021-02405-w
Publication status	Published - Apr 2022

OECD FOS+WOS

1.06.KM GENETICS & HEREDITY

ID: 34866234