XK is a partner for VPS13A: a molecular link between Chorea-Acanthocytosis and McLeod Syndrome-Reference-Cited by-同舟云学术

XK is a partner for VPS13A: a molecular link between Chorea-Acanthocytosis and McLeod Syndrome

Published:2020-10-15 Issue:22 Volume:31 Page:2425-2436
ISSN:1059-1524
Container-title:Molecular Biology of the Cell
language:en
Short-container-title:MBoC

Author:

Park Jae-Sook¹,Neiman Aaron M.¹

Affiliation:

1. Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY 11794-5215

Abstract

Chorea Acanthocytosis and McLeod Syndrome are similar neurodegenerative disorders caused by mutations in the VPS13A and XK genes, respectively. The VPS13A and XK proteins form a complex, suggesting that dysfunction of this complex is the common basis for both diseases.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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4. Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis

5. ER Tubules Mark Sites of Mitochondrial Division

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