Impaired Cytoskeletal and Membrane Biophysical Properties of Acanthocytes in Hypobetalipoproteinemia – A Case Study

Familial hypobetalipoproteinemia is a metabolic disorder mainly caused by mutations in the apolipoprotein B gene. In its homozygous form it can lead without treatment to severe ophthalmological and neurological manifestations. In contrast, the heterozygous form is generally asymptomatic but associat...

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Detalhes bibliográficos
Publicado no:Front Physiol
Main Authors: Cloos, Anne-Sophie, Daenen, Laura G. M., Maja, Mauriane, Stommen, Amaury, Vanderroost, Juliette, Van Der Smissen, Patrick, Rab, Minke, Westerink, Jan, Mignolet, Eric, Larondelle, Yvan, Terrasi, Romano, Muccioli, Giulio G., Dumitru, Andra C., Alsteens, David, van Wijk, Richard, Tyteca, Donatienne
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Physiology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7940373/
https://ncbi.nlm.nih.gov/pubmed/33708142
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2021.638027
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