The Drosophila homolog of MCPH1, a human microcephaly gene, is required for genomic stability in the early embryo.

Mutation of human microcephalin (MCPH1) causes autosomal recessive primary microcephaly, a developmental disorder characterized by reduced brain size. We identified mcph1, the Drosophila homolog of MCPH1, in a genetic screen for regulators of S-M cycles in the early embryo. Embryos of null mcph1 fem...

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Bibliographic Details
Main Authors: Rickmyre, J, Dasgupta, S, Ooi, D, Keel, J, Lee, E, Kirschner, M, Waddell, S, Lee, L
Format: Journal article
Language:English
Published: 2007