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APA Citation
Ramzan, M., Philippe, C., Belyantseva, I. A., Nakano, Y., Fenollar‐Ferrer, C., Tona, R., Yousaf, R., Basheer, R., Imtiaz, A., Faridi, R., Munir, Z., Idrees, H., Salman, M., Nambot, S., Vitobello, A., Kartti, S., Zarrik, O., Witmer, P. D., Sobreria, N., Ibrahimi, A., Banfi, B., Moutton, S., Friedman, T. B., & Naz, S. (2021). variants of human CLDN9 cause mild to profound hearing loss. Human mutation, 42(10), 1321–1335. http://access.bl.uk/ark:/81055/vdc_100142201233.0x000030