Gallant, E., Francey, L., Tsai, E. A., Berman, M., Zhao, Y., Fetting, H., . . . Krantz, I. D. (2013). Homozygosity for the V37I GJB2 Mutation in Fifteen Probands with Mild to Moderate Sensorineural Hearing Impairment: Further Confirmation of Pathogenicity and Haplotype Analysis in Asian Populations.
Chicago-стиль цитированияGallant, Emily, et al. Homozygosity for the V37I GJB2 Mutation in Fifteen Probands With Mild to Moderate Sensorineural Hearing Impairment: Further Confirmation of Pathogenicity and Haplotype Analysis in Asian Populations. 2013.
MLA-цитированиеGallant, Emily, et al. Homozygosity for the V37I GJB2 Mutation in Fifteen Probands With Mild to Moderate Sensorineural Hearing Impairment: Further Confirmation of Pathogenicity and Haplotype Analysis in Asian Populations. 2013.