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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940373/
https://www.ncbi.nlm.nih.gov/pubmed/33708142
http://dx.doi.org/10.3389/fphys.2021.638027

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940373/
https://www.ncbi.nlm.nih.gov/pubmed/33708142
http://dx.doi.org/10.3389/fphys.2021.638027

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