For: | Wu XH, Lin SZ, Zhou YQ, Wang WQ, Li JY, Chen QD. VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report. World J Clin Cases 2022; 10(24): 8749-8754 [PMID: 36157797 DOI: 10.12998/wjcc.v10.i24.8749] |
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URL: | https://www.wjgnet.com/2307-8960/full/v10/i24/8749.htm |
Number | Citing Articles |
1 |
Christina Del Greco, Anthony Antonellis. The Role of Nuclear-Encoded Mitochondrial tRNA Charging Enzymes in Human Inherited Disease. Genes 2022; 13(12): 2319 doi: 10.3390/genes13122319
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2 |
Xiaolu Zhang, Zhengjuan Wu, Xu Zhou, Hua Tao. Mitochondrial dysfunction in epilepsy: mechanistic insights and clinical strategies. Molecular Biology Reports 2025; 52(1) doi: 10.1007/s11033-025-10577-1
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3 |
Shannon Strader, Marissa Vawter‐Lee, Loren Pena, Heather Huxol, Corrie Harris. Why genetic testing is important in patients with developmental disabilities—a unique case of progressive hypertonia and chorea: VARS2‐related disorder. PM&R 2025; 17(3): 344 doi: 10.1002/pmrj.13267
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