CEP152 is a genome maintenance protein disrupted in Seckel syndrome

KALAY, E., YIGIT, G., ASLAN, Y., BROWN, K. E., POHL, E., BICKNELL, L. S., KAYSERILI, H., LI, Y., TUYSUZ, B., NURNBERG, G., KIESS, W., KOEGL, M., BAESSMANN, I., BURUK, K., TORAMAN, B., KAYIPMAZ, S., KUL, S., IKBAL, M., TURNER, D. J., TAYLOR, M. S., AERTS, J., SCOTT, C., MILSTEIN, K., DOLLFUS, Helene, WIECZOREK, D., BRUNNER, H. G., HURLES, M., JACKSON, A. P., RAUCH, A., NURNBERG, P., KARAGUZEL, A. et WOLLNIK, B., 2011. CEP152 is a genome maintenance protein disrupted in Seckel syndrome. Nature Genetics [en ligne]. 2011. Vol. 43, n° 1pp. 23-26. [Consultésans date]. DOI 10.1038/ng.725. Consulté de : http://www.ncbi.nlm.nih.gov/pubmed/21131973