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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

Document Type

Article

Author

Solovyev, A.V.; Teryutin, F.M.; Khusnutdinova, E.K.; Fedorova, S.A.; Pshennikova, V.G.; Barashkov, N.A.; Kushniarevich, A.; Metspalu, E.; Metspalu, M.; Bliznetz, E.; Poliakov, A.; Bady-Khoo, M.; Posukh, O.L.; Lalayants, M.R.; Markova, T.G.; Minárik, G.; Kádasi, L.

Source

In: Human Genetics. (Human Genetics, April 2022, 141(3-4):697-707)

Subject

Language

English

ISSN

14321203
03406717

Online Access

Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Web of Science JCR 저널정보 Scopus Find it@PNU

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