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A novel role for the DNA repair gene Rad51 in Netrin-1 signalling
Mutations in RAD51 have recently been linked to human Congenital Mirror Movements (CMM), a developmental disorder of the motor system. The only gene previously linked to CMM encodes the Netrin-1 receptor DCC, which is important for formation of corticospinal and callosal axon tracts. Thus, we hypoth...
Autores principales: | Glendining, K. A., Markie, D., Gardner, R. J. M., Franz, E. A., Robertson, S. P., Jasoni, C. L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216413/ https://www.ncbi.nlm.nih.gov/pubmed/28057929 http://dx.doi.org/10.1038/srep39823 |
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