Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature

BACKGROUND: Autosomal dominant congenital mirror movements (CMM) is a neurodevelopmental disorder characterized by early onset involuntary movements of one side of the body that mirror intentional movements on the contralateral side; these persist throughout life in the absence of other neurological...

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Detalles Bibliográficos
Autores principales: Trouillard, Oriane, Koht, Jeanette, Gerstner, Thorsten, Moland, Siri, Depienne, Christel, Dusart, Isabelle, Méneret, Aurélie, Ruiz, Marta, Dubacq, Caroline, Roze, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Columbia University Libraries/Information Services 2016
Materias:
Brief Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099496/
https://www.ncbi.nlm.nih.gov/pubmed/27830107
http://dx.doi.org/10.7916/D8BK1CNF

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099496/
https://www.ncbi.nlm.nih.gov/pubmed/27830107
http://dx.doi.org/10.7916/D8BK1CNF

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