APA (7th ed.) Citation

Teryutin, F. M., Pshennikova, V. G., Solovyev, A. V., Romanov, G. P., Fedorova, S. A., & Barashkov, N. A. Genotype-phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26). Public Library of Science (PLoS).

Chicago Style (17th ed.) Citation

Teryutin, Fedor M., Vera G. Pshennikova, Aisen V. Solovyev, Georgii P. Romanov, Sardana A. Fedorova, and Nikolay A. Barashkov. Genotype-phenotype Analysis of Hearing Function in Patients with DFNB1A Caused by the C.-23+1G>A Splice Site Variant of the GJB2 Gene (Cx26). Public Library of Science (PLoS).

MLA (9th ed.) Citation

Teryutin, Fedor M., et al. Genotype-phenotype Analysis of Hearing Function in Patients with DFNB1A Caused by the C.-23+1G>A Splice Site Variant of the GJB2 Gene (Cx26). Public Library of Science (PLoS).