Heeringa, S.F., Chernin, G., Chaki, M., Zhou, W., Sloan, A.J., Ji, Z., Xie, L.X., Salviati, L., Hurd, T.W., Vega-Warner, V., Killen, P.D., Raphael, Y., Ashraf, S., Ovunc, B., Schoeb, D.S., McLaughlin, H.M., Airik, R., Vlangos, C.N., Gbadegesin, R., Hinkes, B., Saisawat, P., Trevisson, E., Doimo, M., Casarin, A., Pertegato, V., Giorgi, G., Prokisch, H., Rötig, A., Nürnberg, G., Becker, C., Wang, S., Ozaltin, F., Topaloglu, R., Bakkaloglu, A., Bakkaloglu, S.A., Müller, D., Beissert, A., Mir, S., Berdeli, A., Varpizen, S., Zenker, M., Matejas, V., Santos-Ocaña, C., Navas, P., Kusakabe, T., Kispert, A., Akman, S., Soliman, N.A., Krick, S., Mundel, P., Reiser, J., Nürnberg, P., Clarke, C.F., Wiggins, R.C., Faul, C., and Hildebrandt, F. (2011) COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J. Clin. Invest.. 121(5):2013-2024

Heeringa, S.F., Chernin, G., Chaki, M., Zhou, W., Sloan, A.J., Ji, Z., Xie, L.X., Salviati, L., Hurd, T.W., Vega-Warner, V., Killen, P.D., Raphael, Y., Ashraf, S., Ovunc, B., Schoeb, D.S., McLaughlin, H.M., Airik, R., Vlangos, C.N., Gbadegesin, R., Hinkes, B., Saisawat, P., Trevisson, E., Doimo, M., Casarin, A., Pertegato, V., Giorgi, G., Prokisch, H., Rötig, A., Nürnberg, G., Becker, C., Wang, S., Ozaltin, F., Topaloglu, R., Bakkaloglu, A., Bakkaloglu, S.A., Müller, D., Beissert, A., Mir, S., Berdeli, A., Varpizen, S., Zenker, M., Matejas, V., Santos-Ocaña, C., Navas, P., Kusakabe, T., Kispert, A., Akman, S., Soliman, N.A., Krick, S., Mundel, P., Reiser, J., Nürnberg, P., Clarke, C.F., Wiggins, R.C., Faul, C., and Hildebrandt, F. (2011) COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J. Clin. Invest.. 121(5):2013-2024