MCPH1, mutated in primary microcephaly, is required for efficient chromosome alignment during mitosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-12793-7.pdf
Reference29 articles.
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2. Thornton, G. K. & Woods, C. G. Primary microcephaly: do all roads lead to Rome? Trends Genet. 25, 501–10, https://doi.org/10.1016/j.tig.2009.09.011 (2009).
3. Mahmood, S., Ahmad, W. & Hassan, M. J. Autosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum. Orphanet J Rare Dis. 6, 39, https://doi.org/10.1186/1750-1172-6-39 (2011).
4. Barbelanne, M. & Tsang, W. Y. Molecular and cellular basis of autosomal recessive primary microcephaly. Biomed Res Int. 2014: 547986, https://doi.org/10.1155/2014/547986 (2014).
5. Khan, M. A. et al. A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family. Hum Mol Genet. 23, 5940–9, https://doi.org/10.1093/hmg/ddu318 (2014).
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