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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Tremor Other Hyperkinet Mov (N Y)
Autors principals: Trouillard, Oriane, Koht, Jeanette, Gerstner, Thorsten, Moland, Siri, Depienne, Christel, Dusart, Isabelle, Méneret, Aurélie, Ruiz, Marta, Dubacq, Caroline, Roze, Emmanuel
Format: Artigo
Idioma:Inglês
Publicat: Columbia University Libraries/Information Services 2016
Matèries:
Brief Reports
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5099496/
https://ncbi.nlm.nih.gov/pubmed/27830107
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7916/D8BK1CNF
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars