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Comment
. 2011 May;79(5):428-30.
doi: 10.1111/j.1399-0004.2011.01655.x. Epub 2011 Mar 13.

Step to CEP152: uncovering a new mutation implicated in Seckel syndrome

S Ladha  1
Affiliations
Comment

Step to CEP152: uncovering a new mutation implicated in Seckel syndrome

S Ladha. Clin Genet. 2011 May.
No abstract available

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Comment on

  • CEP152 is a genome maintenance protein disrupted in Seckel syndrome.
    Kalay E, Yigit G, Aslan Y, Brown KE, Pohl E, Bicknell LS, Kayserili H, Li Y, Tüysüz B, Nürnberg G, Kiess W, Koegl M, Baessmann I, Buruk K, Toraman B, Kayipmaz S, Kul S, Ikbal M, Turner DJ, Taylor MS, Aerts J, Scott C, Milstein K, Dollfus H, Wieczorek D, Brunner HG, Hurles M, Jackson AP, Rauch A, Nürnberg P, Karagüzel A, Wollnik B. Kalay E, et al. Nat Genet. 2011 Jan;43(1):23-6. doi: 10.1038/ng.725. Epub 2010 Dec 5. Nat Genet. 2011. PMID: 21131973 Free PMC article.

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