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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Detalles Bibliográficos
Autores principales: Finnsson, Johannes, Lubberink, Mark, Savitcheva, Irina, Fällmar, David, Melberg, Atle, Kumlien, Eva, Raininko, Raili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585974/
https://www.ncbi.nlm.nih.gov/pubmed/30192380
http://dx.doi.org/10.1111/ane.13024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585974/
https://www.ncbi.nlm.nih.gov/pubmed/30192380
http://dx.doi.org/10.1111/ane.13024

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