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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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Aisen V. Solovyev
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Aleksandra M. Cherdonova
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Fedor M. Teryutin
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Georgii P. Romanov
Leonid A. Klarov
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Nikolay A. Barashkov
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Nikolay V. Luginov
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Petr M. Kotlyarov
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Vera G. Pshennikova
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FOXI1
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KCNJ10 genes
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SLC26A4
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audiometric examination
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computer tomography
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hearing loss
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incomplete partition type 1 (IP-1)
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inner ear anomalies
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Biology (General)
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Chemistry
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DFNB4
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Eastern Siberia
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Pendred syndrome
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QD1-999
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QH301-705.5
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Russia
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enlarged vestibular aqueduct (EVA)
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genotype-phenotype analysis
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incomplete partition type 2 (IP-2)
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Directory of Open Access Journals: DOAJ Articles
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Sakha
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Sakha Republic
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Siberia
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