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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Biomedicine and Life Sciences
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

Internet

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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