A partnership between the lipid scramblase XK and the lipid transfer protein VPS13A at the plasma membrane

Chorea-acanthocytosis (ChAc) and McLeod syndrome are diseases with shared clinical manifestations caused by mutations in VPS13A and XK, respectively. Key features of these conditions are the degeneration of caudate neurons and the presence of abnormally shaped erythrocytes. XK belongs to a family of...

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Detalles Bibliográficos
Autores principales: Guillén-Samander, Andrés, Wu, Yumei, Pineda, S. Sebastian, García, Francisco J., Eisen, Julia N., Leonzino, Marianna, Ugur, Berrak, Kellis, Manolis, Heiman, Myriam, De Camilli, Pietro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Biological Sciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436381/
https://www.ncbi.nlm.nih.gov/pubmed/35994651
http://dx.doi.org/10.1073/pnas.2205425119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436381/
https://www.ncbi.nlm.nih.gov/pubmed/35994651
http://dx.doi.org/10.1073/pnas.2205425119

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