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LMNB1‐related autosomal‐dominant leukodystrophy: Clinical and radiological course
OBJECTIVE: Duplication of the LMNB1 gene encoding lamin B1 causes adult‐onset autosomal‐dominant leukodystrophy (ADLD) starting with autonomic symptoms, which are followed by pyramidal signs and ataxia. Magnetic resonance imaging (MRI) of the brain reveals characteristic findings. This is the first...
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| Gepubliceerd in: | Ann Neurol |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5054845/ https://ncbi.nlm.nih.gov/pubmed/26053668 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24452 |
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