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Maekawa K, Nishio S-y, Abe S, Goto S-i, Honkura Y, Iwasaki S, Kanda Y, Kobayashi Y, Oka S-i, Okami M, et al. Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort. Genes. 2019; 10(10):735. https://doi.org/10.3390/genes10100735

Maekawa, Karuna, Shin-ya Nishio, Satoko Abe, Shin-ichi Goto, Yohei Honkura, Satoshi Iwasaki, Yukihiko Kanda, Yumiko Kobayashi, Shin-ichiro Oka, Mayuri Okami, and et al. 2019. "Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort" Genes 10, no. 10: 735. https://doi.org/10.3390/genes10100735

Maekawa, K., Nishio, S.-y., Abe, S., Goto, S.-i., Honkura, Y., Iwasaki, S., Kanda, Y., Kobayashi, Y., Oka, S.-i., Okami, M., Oshikawa, C., Sakuma, N., Sano, H., Shirakura, M., Uehara, N., & Usami, S.-i. (2019). Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort. Genes, 10(10), 735. https://doi.org/10.3390/genes10100735