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APA Citation
Van Laer, L., Coucke, P., Mueller, R. F., Caethoven, G., Flothmann, K., Prasad, S. D., Chamberlin, G. P., Houseman, M., Taylor, G. R., Van de Heyning, C. M., Fransen, E., Rowland, J., Cucci, R. A., Smith, R. J. H., & Van Camp, G. (2001). a common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment. Journal of medical genetics, 38(8), 515–518. http://access.bl.uk/ark:/81055/vdc_100137792695.0x000038