Hidalgo‐Gutierrez, A., Shintaku, J., Ramon, J., Barriocanal‐Casado, E., Pesini, A., Saneto, R. P., Garrabou, G., Milisenda, J. C., Matas‐Garcia, A., Gort, L., Ugarteburu, O., Gu, Y., Koganti, L., Wang, T., Tadesse, S., Meneri, M., Sciacco, M., Wang, S., Tanji, K., … Hirano, M. (2024). Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease. Annals of Neurology, 96(6), 1209–1224. Portico. https://doi.org/10.1002/ana.27071
Subjects:
DNA, Mitochondrial
(MeSH)
Mitochondrial Dynamics and Reactive Oxygen Species Regulation
(OpenAlex Topic)
Metabolic Disorders and Biochemical Genetics
(OpenAlex Topic)
Nucleotide Metabolism and Enzyme Regulation
(OpenAlex Topic)
Publication Type:
Article
Unique ID:
10.1002/ana.27071
PMID:
DOI:
Journal:
Publication Date:
Data Source:
OpenAlex