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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Dettagli Bibliografici
Pubblicato in:Front Physiol
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2021
Soggetti:
Physiology
Accesso online: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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