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Mitochondrial DNA depletion syndrome with a mutation in SLC25A4 developing epileptic encephalopathy: A case report.
Brain Dev. 2022 Jan;44(1):56-62. doi: 10.1016/j.braindev.2021.08.005. Epub 2021 Aug 25.
Brain Dev. 2022.
PMID: 34452803
Effect of Flunarizine on Alternating Hemiplegia of Childhood in a Patient with the p.E815K Mutation in ATP1A3: A Case Report.
Kusunoki S, Kido J, Momosaki K, Sawada T, Kashiki T, Matsumoto S, Nakamura K.
Kusunoki S, et al.
Case Rep Neurol. 2020 Sep 18;12(3):299-306. doi: 10.1159/000509287. eCollection 2020 Sep-Dec.
Case Rep Neurol. 2020.
PMID: 33082768
Free PMC article.
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