CEP152 is a genome maintenance protein disrupted in Seckel syndrome

Ersan Kalay(Karadeniz Technical University), Gökhan Yigit(University of Cologne), Yakup Aslan(Karadeniz Technical University), Karen Brown(Hammersmith Hospital), Esther Pohl(University of Cologne), Louise S. Bicknell(Western General Hospital), Hülya Kayserili(Istanbul University), Yun Li(University of Cologne), Beyhan Tüysüz(Istanbul University), Gudrun Nürnberg(University of Cologne), Wieland Kieß, Manfred Koegl(German Cancer Research Center), Ingelore Baessmann(University of Cologne), Celal Kurtuluş Buruk(Karadeniz Technical University), Bayram Toraman(Karadeniz Technical University), Saadettin Kayıpmaz(Karadeniz Technical University), Sibel Kul(Karadeniz Technical University), Mevlit Íkbal(Karadeniz Technical University), Daniel J. Turner(Wellcome Sanger Institute), Martin S. Taylor(Western General Hospital), Jan Aerts(Wellcome Sanger Institute), Carol Scott(Wellcome Sanger Institute), Karen Milstein(National Health Laboratory Service), Hélène Dollfus(Hôpitaux Universitaires de Strasbourg), Dagmar Wieczorek(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Han G. Brunner(Radboud University Nijmegen), Matthew E. Hurles(Wellcome Sanger Institute), Andrew P. Jackson(Western General Hospital), Anita Rauch, Peter Nürnberg(University of Cologne), Ahmet Karagüzel(Karadeniz Technical University), Bernd Wollnik(University of Cologne)
Nature Genetics
December 5, 2010
Cited by 225Open Access
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