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 mcphl, the Drosophila homolog of MCPH1, in a genetic screen for regulators of S-M cycles in the early embryo. Embryos of null mcph1 fem...
Huvudupphovsmän: | , , , , , , , |
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Materialtyp: | Journal article |
Språk: | English |
Publicerad: |
2007
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The Drosophila homolog of MCPH1, a human microcephaly gene, is required for genomic stability in the early embryo.
Publicerad 2007
Journal article