Human ASPM participates in spindle organisation, spindle orientation and cytokinesis

<p>Abstract</p> <p>Background</p> <p>Mutations in the Abnormal Spindle Microcephaly related gene (<it>ASPM) </it>are the commonest cause of autosomal recessive primary microcephaly (MCPH) a disorder characterised by a small brain and associated mental retard...

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Bibliographic Details
Main Authors: Woods C Geoffrey, Glover David M, Bennett Christopher, Sharif Saghira M, Binns Ruth K, Roberts Emma, Askham Jonathan M, Bell Sandra M, Bergh Anna-Maria, Midgley Carol, Higgins Julie, Morrison Ewan E, Bond Jacquelyn
Format: Article
Language:English
Published: BMC 2010-11-01
Series:BMC Cell Biology
Online Access:http://www.biomedcentral.com/1471-2121/11/85