Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations-Reference-Cited by-同舟云学术

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Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations

Published:2013-10-23 Issue:21 Volume:81 Page:1810-1818
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Aure K.,Dubourg O.,Jardel C.,Clarysse L.,Sternberg D.,Fournier E.,Laforet P.,Streichenberger N.,Petiot P.,Gervais-Bernard H.,Vial C.,Bedat-Millet A.-L.,Drouin-Garraud V.,Bouillaud F.,Vandier C.,Fontaine B.,Lombes A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 50 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Variability of Clinical Phenotypes Caused by Isolated Defects of Mitochondrial ATP Synthase;Physiological Research;2024-08-31

2. Variants in Human ATP Synthase Mitochondrial Genes: Biochemical Dysfunctions, Associated Diseases, and Therapies;International Journal of Molecular Sciences;2024-02-13

3. Hereditary Motor Neuropathy;Reference Module in Neuroscience and Biobehavioral Psychology;2024

4. Episodic flaccid muscle weakness (Periodic paralysis);Neurogenetics for the Practitioner;2024

5. Analysis of MT-ATP8 gene variants reported in patients by modeling in silico and in yeast model organism;Scientific Reports;2023-06-20

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