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APA Citation
Kari, E., Llaci, L., Go, J. L., Naymik, M., Knowles, J. A., Leal, S. M., Rangasamy, S., Huentelman, M. J., Friedman, R. A., & Schrauwen, I. (2019). a de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing loss. Molecular genetics & genomic medicine, 7(12), n/a. http://access.bl.uk/ark:/81055/vdc_100098072536.0x00000d