CEP152 is a genome maintenance protein disrupted in Seckel syndrome.

Autor: Kalay, Ersan1,2,3 ersankalay@hotmail.com, Yigit, Gökhan2,3,4, Aslan, Yakup5, Brown, Karen E.6, Pohl, Esther2,3, Bicknell, Louise S.7, Kayserili, Hülya8, Yun Li2,3, Tüysüz, Beyhan9, Nürnberg, Gudrun3,4,10, Kiess, Wieland11, Koegl, Manfred12, Baessmann, Ingelore3,10, Buruk, Kurtulus13, Toraman, Bayram1, Kayipmaz, Saadettin14, Kul, Sibel15, Ikbal, Mevlit16, Turner, Daniel J.17, Taylor, Martin S.7
Zdroj: Nature Genetics. Jan2011, Vol. 43 Issue 1, p23-26. 4p. 1 Color Photograph, 1 Graph.
Databáze: Academic Search Ultimate