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...
Main Authors: | , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2010-11-01
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Series: | BMC Cell Biology |
Online Access: | http://www.biomedcentral.com/1471-2121/11/85 |