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Microcephalin/MCPH1 Associates with the Condensin II Complex to Function in Homologous Recombination Repair
Microcephalin/MCPH1 is one of the causative genes responsible for the autosomal recessive disorder primary microcephaly. Patients with this disease present with mental retardation and dramatic reduction in head size, and cells derived from these patients contain abnormally condensed chromosomes. MCP...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2570891/ https://ncbi.nlm.nih.gov/pubmed/18718915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M804080200 |
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