VPS13A and VPS13C are lipid transport proteins differentially localized at ER contact sites

Mutations in the human VPS13 genes are responsible for neurodevelopmental and neurodegenerative disorders including chorea acanthocytosis (VPS13A) and Parkinson’s disease (VPS13C). The mechanisms of these diseases are unknown. Genetic studies in yeast hinted that Vps13 may have a role in lipid excha...

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Detalles Bibliográficos
Autores principales: Kumar, Nikit, Leonzino, Marianna, Hancock-Cerutti, William, Horenkamp, Florian A., Li, PeiQi, Lees, Joshua A., Wheeler, Heather, Reinisch, Karin M., De Camilli, Pietro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168267/
https://www.ncbi.nlm.nih.gov/pubmed/30093493
http://dx.doi.org/10.1083/jcb.201807019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168267/
https://www.ncbi.nlm.nih.gov/pubmed/30093493
http://dx.doi.org/10.1083/jcb.201807019

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