Učitavanje...
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...
Spremljeno u:
| Izdano u: | Acta Neurol Scand |
|---|---|
| Glavni autori: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
John Wiley and Sons Inc.
2018
|
| Teme: | |
| Online pristup: | 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 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|