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Glucose metabolism in the brain in LMNB1‐related autosomal dominant leukodystrophy
OBJECTIVE: LMNB1‐related autosomal dominant leukodystrophy is caused by an overexpression of the protein lamin B1, usually due to a duplication of the LMNB1 gene. Symptoms start in 5(th) to 6(th) decade. This slowly progressive disease terminates with death. We studied brain glucose metabolism in th...
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| Pubblicato in: | Acta Neurol Scand |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6585974/ https://ncbi.nlm.nih.gov/pubmed/30192380 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ane.13024 |
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