Kim, H.-G., J.-W. Ahn, I. Kurth, R. Ullmann, H.-T. Kim, A. Kulharya, K.-S. Ha, Y. Itokawa, I. Meliciani, W. W. Wolfgang Wenzel, D. Lee, G. Rosenberger, M. Ozata, D. P. Bick, R. J. Sherins, T. Nagase, M. Tekin, S.-H. Kim, C.-H. Kim, H.-H. Ropers, J. F. Gusella, V. M. Kalscheuer, C. Y. Choi and L. C. Layman: WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.. In: American Society of Human Genetics 87, 4, 465-479 (2010).
url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756557/pdf/main.pdf
doi: 10.1016/j.ajhg.2010.08.018
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