The Hexokinase 1 5′-UTR Mutation in Charcot–Marie–Tooth 4G Disease Alters Hexokinase 1 Binding to Voltage-Dependent Anion Channel-1 and Leads to Dysfunctional Mitochondrial Calcium Buffering.

Autor: Ceprian, Maria1 (AUTHOR) maria.ceprian@achucarro.org, Juntas-Morales, Raul2,3 (AUTHOR) raul.juntas@vallhebron.cat, Campbell, Graham1 (AUTHOR), Walther-Louvier, Ulrike4 (AUTHOR) u-louvier@chu-montpellier.fr, Rivier, François4 (AUTHOR) f-rivier@chu-montpellier.fr, Camu, William2 (AUTHOR) w-camu@chu-montpellier.fr, Esselin, Florence2 (AUTHOR) f-esselin@chu-montpellier.fr, Echaniz-Laguna, Andoni5 (AUTHOR) andoni.echaniz-laguna@aphp.fr, Stojkovic, Tanya6 (AUTHOR) tanya.stojkovic@aphp.fr, Bouhour, Françoise7 (AUTHOR) francoise.bouhour@chu-lyon.fr, Latour, Philippe8 (AUTHOR) philippe.latour@chu-lyon.fr, Tricaud, Nicolas1,9 (AUTHOR) nicolas.tricaud@inserm.fr
Zdroj: International Journal of Molecular Sciences. Apr2024, Vol. 25 Issue 8, p4364. 12p.
Databáze: Academic Search Ultimate
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