Borck, G., Rehman, A.U., Lee, K., Pogoda, H.M., Kakar, N., von Ameln, S., Grillet, N., Hildebrand, M.S., Ahmed, Z.M., Nürnberg, G., Ansar, M., Basit, S., Javed, Q., Morell, R.J., Nasreen, N., Shearer, A.E., Ahmad, A., Kahrizi, K., Shaikh, R.S., Ali, R.A., Khan, S.N., Goebel, I., Meyer, N.C., Kimberling, W.J., Webster, J.A., Stephan, D.A., Schiller, M.R., Bahlo, M., Najmabadi, H., Gillespie, P.G., Nürnberg, P., Wollnik, B., Riazuddin, S., Smith, R.J., Ahmad, W., Müller, U., Hammerschmidt, M., Friedman, T.B., Riazuddin, S., Leal, S.M., Ahmad, J., and Kubisch, C. (2011) Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42. American journal of human genetics. 88(2):127-137

Strausberg,R.L., Feingold,E.A., Grouse,L.H., Derge,J.G., Klausner,R.D., Collins,F.S., Wagner,L., Shenmen,C.M., Schuler,G.D., Altschul,S.F., Zeeberg,B., Buetow,K.H., Schaefer,C.F., Bhat,N.K., Hopkins,R.F., Jordan,H., Moore,T., Max,S.I., Wang,J., Hsieh,F., Diatchenko,L., Marusina,K., Farmer,A.A., Rubin,G.M., Hong,L., Stapleton,M., Soares,M.B., Bonaldo,M.F., Casavant,T.L., Scheetz,T.E., Brownstein,M.J., Usdin,T.B., Toshiyuki,S., Carninci,P., Prange,C., Raha,S.S., Loquellano,N.A., Peters,G.J., Abramson,R.D., Mullahy,S.J., Bosak,S.A., McEwan,P.J., McKernan,K.J., Malek,J.A., Gunaratne,P.H., Richards,S., Worley,K.C., Hale,S., Garcia,A.M., Gay,L.J., Hulyk,S.W., Villalon,D.K., Muzny,D.M., Sodergren,E.J., Lu,X., Gibbs,R.A., Fahey,J., Helton,E., Ketteman,M., Madan,A., Rodrigues,S., Sanchez,A., Whiting,M., Madan,A., Young,A.C., Shevchenko,Y., Bouffard,G.G., Blakesley,R.W., Touchman,J.W., Green,E.D., Dickson,M.C., Rodriguez,A.C., Grimwood,J., Schmutz,J., Myers,R.M., Butterfield,Y.S., Krzywinski,M.I., Skalska,U., Smailus,D.E., Schnerch,A., Schein,J.E., Jones,S.J., and Marra,M.A. (2002) Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 99(26):16899-903

Borck, G., Rehman, A.U., Lee, K., Pogoda, H.M., Kakar, N., von Ameln, S., Grillet, N., Hildebrand, M.S., Ahmed, Z.M., Nürnberg, G., Ansar, M., Basit, S., Javed, Q., Morell, R.J., Nasreen, N., Shearer, A.E., Ahmad, A., Kahrizi, K., Shaikh, R.S., Ali, R.A., Khan, S.N., Goebel, I., Meyer, N.C., Kimberling, W.J., Webster, J.A., Stephan, D.A., Schiller, M.R., Bahlo, M., Najmabadi, H., Gillespie, P.G., Nürnberg, P., Wollnik, B., Riazuddin, S., Smith, R.J., Ahmad, W., Müller, U., Hammerschmidt, M., Friedman, T.B., Riazuddin, S., Leal, S.M., Ahmad, J., and Kubisch, C. (2011) Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42. American journal of human genetics. 88(2):127-137

Strausberg,R.L., Feingold,E.A., Grouse,L.H., Derge,J.G., Klausner,R.D., Collins,F.S., Wagner,L., Shenmen,C.M., Schuler,G.D., Altschul,S.F., Zeeberg,B., Buetow,K.H., Schaefer,C.F., Bhat,N.K., Hopkins,R.F., Jordan,H., Moore,T., Max,S.I., Wang,J., Hsieh,F., Diatchenko,L., Marusina,K., Farmer,A.A., Rubin,G.M., Hong,L., Stapleton,M., Soares,M.B., Bonaldo,M.F., Casavant,T.L., Scheetz,T.E., Brownstein,M.J., Usdin,T.B., Toshiyuki,S., Carninci,P., Prange,C., Raha,S.S., Loquellano,N.A., Peters,G.J., Abramson,R.D., Mullahy,S.J., Bosak,S.A., McEwan,P.J., McKernan,K.J., Malek,J.A., Gunaratne,P.H., Richards,S., Worley,K.C., Hale,S., Garcia,A.M., Gay,L.J., Hulyk,S.W., Villalon,D.K., Muzny,D.M., Sodergren,E.J., Lu,X., Gibbs,R.A., Fahey,J., Helton,E., Ketteman,M., Madan,A., Rodrigues,S., Sanchez,A., Whiting,M., Madan,A., Young,A.C., Shevchenko,Y., Bouffard,G.G., Blakesley,R.W., Touchman,J.W., Green,E.D., Dickson,M.C., Rodriguez,A.C., Grimwood,J., Schmutz,J., Myers,R.M., Butterfield,Y.S., Krzywinski,M.I., Skalska,U., Smailus,D.E., Schnerch,A., Schein,J.E., Jones,S.J., and Marra,M.A. (2002) Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 99(26):16899-903