CEP152 is a genome maintenance protein disrupted in Seckel syndrome-Reference-Cited by-同舟云学术

CEP152 is a genome maintenance protein disrupted in Seckel syndrome

Published:2010-12-05 Issue:1 Volume:43 Page:23-26
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Kalay Ersan,Yigit Gökhan,Aslan Yakup,Brown Karen E,Pohl Esther,Bicknell Louise S,Kayserili Hülya,Li Yun,Tüysüz Beyhan,Nürnberg Gudrun,Kiess Wieland,Koegl Manfred,Baessmann Ingelore,Buruk Kurtulus,Toraman Bayram,Kayipmaz Saadettin,Kul Sibel,Ikbal Mevlit,Turner Daniel J,Taylor Martin S,Aerts Jan,Scott Carol,Milstein Karen,Dollfus Helene,Wieczorek Dagmar,Brunner Han G,Hurles Matthew,Jackson Andrew P,Rauch Anita,Nürnberg Peter,Karagüzel Ahmet,Wollnik Bernd

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.725.pdf

Reference15 articles.

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4. O'Driscoll, M., Ruiz-Perez, V.L., Woods, C.G., Jeggo, P.A. & Goodship, J.A. Nat. Genet. 33, 497–501 (2003).

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