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APA Citation
Macnamara, E. F., Koehler, A. E., D'Souza, P., Estwick, T., Lee, P., Vezina, G., , , Fauni, H., Braddock, S. R., Torti, E., Holt, J. M., Sharma, P., Malicdan, M. C. V., & Tifft, C. J. (2019). kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2. Human mutation, 40(5), 532–538. http://access.bl.uk/ark:/81055/vdc_100080203974.0x000030