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Comment
. 2011 Sep;80(3):241-2.
doi: 10.1111/j.1399-0004.2011.01753.x.

The essential role of NDE1 in extreme microcephaly

M Ghannad  1
Affiliations
Comment

The essential role of NDE1 in extreme microcephaly

M Ghannad. Clin Genet. 2011 Sep.
No abstract available

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Comment on

  • Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
    Alkuraya FS, Cai X, Emery C, Mochida GH, Al-Dosari MS, Felie JM, Hill RS, Barry BJ, Partlow JN, Gascon GG, Kentab A, Jan M, Shaheen R, Feng Y, Walsh CA. Alkuraya FS, et al. Am J Hum Genet. 2011 May 13;88(5):536-47. doi: 10.1016/j.ajhg.2011.04.003. Epub 2011 Apr 28. Am J Hum Genet. 2011. PMID: 21529751 Free PMC article.
  • The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.
    Bakircioglu M, Carvalho OP, Khurshid M, Cox JJ, Tuysuz B, Barak T, Yilmaz S, Caglayan O, Dincer A, Nicholas AK, Quarrell O, Springell K, Karbani G, Malik S, Gannon C, Sheridan E, Crosier M, Lisgo SN, Lindsay S, Bilguvar K, Gergely F, Gunel M, Woods CG. Bakircioglu M, et al. Am J Hum Genet. 2011 May 13;88(5):523-35. doi: 10.1016/j.ajhg.2011.03.019. Epub 2011 Apr 28. Am J Hum Genet. 2011. PMID: 21529752 Free PMC article.

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