Human ASPM participates in spindle organisation, spindle orientation and cytokinesis

BACKGROUND: Mutations in the Abnormal Spindle Microcephaly related gene (ASPM) are the commonest cause of autosomal recessive primary microcephaly (MCPH) a disorder characterised by a small brain and associated mental retardation. ASPM encodes a mitotic spindle pole associated protein. It is suggest...

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Bibliografische gegevens
Hoofdauteurs: Higgins, Julie, Midgley, Carol, Bergh, Anna-Maria, Bell, Sandra M, Askham, Jonathan M, Roberts, Emma, Binns, Ruth K, Sharif, Saghira M, Bennett, Christopher, Glover, David M, Woods, C Geoffrey, Morrison, Ewan E, Bond, Jacquelyn
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2010
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2988714/
https://ncbi.nlm.nih.gov/pubmed/21044324
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2121-11-85
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