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Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies.
Int J Mol Sci. 2022 Dec 6;23(23):15372. doi: 10.3390/ijms232315372.
Int J Mol Sci. 2022.
PMID: 36499699
Free PMC article.
A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia.
Romanov GP, Pshennikova VG, Lashin SA, Solovyev AV, Teryutin FM, Cherdonova AM, Borisova TV, Sazonov NN, Khusnutdinova EK, Posukh OL, Fedorova SA, Barashkov NA.
Romanov GP, et al. Among authors: cherdonova am.
PLoS One. 2020 Nov 30;15(11):e0242219. doi: 10.1371/journal.pone.0242219. eCollection 2020.
PLoS One. 2020.
PMID: 33253245
Free PMC article.
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