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Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control
Mirror movements (MM) disorder is characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side. We performed genetic characterization of a family with autosomal dominant MM and identified ARHGEF7, a RhoGEF, as a candidate MM gene. We found tha...
Autores principales: | Schlienger, Sabrina, Yam, Patricia T., Balekoglu, Nursen, Ducuing, Hugo, Michaud, Jean-Francois, Makihara, Shirin, Kramer, Daniel K., Chen, Baoyu, Fasano, Alfonso, Berardelli, Alfredo, Hamdan, Fadi F., Rouleau, Guy A., Srour, Myriam, Charron, Frederic |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10181192/ https://www.ncbi.nlm.nih.gov/pubmed/37172092 http://dx.doi.org/10.1126/sciadv.add5501 |
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