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Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive
Deafness
1A (DFNB1A)
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Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive
Deafness
1A (DFNB1A)
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Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive
Deafness
1A (DFNB1A)
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Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete...
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Analysis of SLC26A4,FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete...
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Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete...
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Reconstruction of the founder haplotype with mutation c.1621C>T (p.Gln541*) in t...
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Novel transition c.1621C>T (p.Gln541*) in the FYCO1 gene is a major cause of con...
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5
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3
Author
Fedor M. Teryutin
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Georgii P. Romanov
4
Nikolay A. Barashkov
4
Vera G. Pshennikova
4
Aisen V. Solovyev
2
Aisen V. Solov’ev
2
Aleksandra M. Cherdonova
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Alena A. Nikanorova
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Alexander A. Bondar
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Barashkov, Nikolay A.
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Elza K. Khusnutdinova
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Igor V. Morozov
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Leonid A. Klarov
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Lilya U. Dzhemileva
2
Nikolay N. Sazonov
2
Nikolay V. Luginov
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Nyurgun N. Gotovtsev
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Olga L. Posukh
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Petr M. Kotlyarov
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Pshennikova, Vera G.
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Romanov, Georgii P.
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Sardana A. Fedorova
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Sergey S. Nakhodkin
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Teryutin, Fedor M.
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A. V. Solovyev
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Eastern Siberia
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CTRCT18
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FOXI1
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FYCO1
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KCNJ10 genes
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SLC26A4
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Yakuts
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audiometric examination
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computer tomography
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congenital autosomal recessive cataract
2
hearing loss
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incomplete partition type 1 (IP-1)
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inner ear anomalies
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population isolate
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Восточная Сибирь
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ген FYCO1
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популяционный изолят
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якуты
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Biology (General)
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DFNB4
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Pendred syndrome
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QH301-705.5
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R
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Directory of Open Access Journals: DOAJ Articles
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PubMed Central (PMC)
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Hindawi Publishing Corporation
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MDPI Open Access Publishing
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Sakha
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