“CEP63 deficiency promote p53 dependent microcephaly and reveals a role for the centrosome in meiotic recombination”. Travis H.Stracker

Thursday, November 6, 2014

Mutations in human CEP63 centrosome protein cause Seckel syndrome, characterized by growth retardation and microencephaly. In mice deficient for CEP63, which recapitulate the human pathology, cell death seems…

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