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Adult-Onset Vanishing White Matter Disease Due to a Novel EIF2B3 Mutation
OBJECTIVE: To report a novel mutation in the gene EIF2B3 responsible for a late-onset form of vanishing white matter disease. DESIGN: Case report. SETTING: University teaching hospital. PATIENT: A 29-year-old pregnant woman with a history of premature ovarian failure and hemiplegic migraines present...
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| Hauptverfasser: | , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2012
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4154510/ https://ncbi.nlm.nih.gov/pubmed/22312164 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2011.1942 |
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