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Title
Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations
Authors
Keywords
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Journal
Frontiers in Neurology
Volume 10, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2019-05-08
DOI
10.3389/fneur.2019.00496
References
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- Leigh syndrome: One disorder, more than 75 monogenic causes
- (2015) Nicole J. Lake et al. ANNALS OF NEUROLOGY
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- Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlations
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- A multicenter study on Leigh syndrome: disease course and predictors of survival
- (2014) Kalliopi Sofou et al. Orphanet Journal of Rare Diseases
- Mitochondrial epilepsy in pediatric and adult patients
- (2013) J. Finsterer et al. ACTA NEUROLOGICA SCANDINAVICA
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- (2008) D. Khurana et al. NEUROPEDIATRICS
- Leigh and Leigh-Like Syndrome in Children and Adults
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