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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

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
Human Genetics · Vol. 141, Issue 3-4 · pp. 697-707 · 2022
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2022-04-01
Publication Year2022
Volume141
Issue3-4
Pages697-707
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-021-02405-w

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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