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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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| Vydáno v: | Tremor Other Hyperkinet Mov (N Y) |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Columbia University Libraries/Information Services
2016
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| Témata: | |
| On-line přístup: | 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 |
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