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Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations.
Clin Neurol Neurosurg. 2018 Jan;164:182-189. doi: 10.1016/j.clineuro.2017.12.010. Epub 2017 Dec 9.
Clin Neurol Neurosurg. 2018.
PMID: 29272804
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
Chakrabarty S, Govindaraj P, Sankaran BP, Nagappa M, Kabekkodu SP, Jayaram P, Mallya S, Deepha S, Ponmalar JNJ, Arivinda HR, Meena AK, Jha RK, Sinha S, Gayathri N, Taly AB, Thangaraj K, Satyamoorthy K.
Chakrabarty S, et al. Among authors: ponmalar jnj.
J Neurol. 2021 Jun;268(6):2192-2207. doi: 10.1007/s00415-020-10390-9. Epub 2021 Jan 23.
J Neurol. 2021.
PMID: 33484326
Free PMC article.
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