A Chinese Family With Adult-Onset Leigh-Like Syndrome Caused by the Heteroplasmic m.10191T>C Mutation in the Mitochondrial MTND3 Gene

Management of Leigh syndrome: Current status and new insights

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Mitochondrial medicine in the omics era

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Mitochondrial DNA mutations in late-onset Leigh syndrome

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Leigh syndrome in individuals bearing m.9185T>C MTATP6 variant. Is hyperventilation a factor which starts its development?

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Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options

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Mitochondrial diseases

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Leigh syndrome: One disorder, more than 75 monogenic causes

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Mutations causing mitochondrial disease: What is new and what challenges remain?

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The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia

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Long Survival in Patients With Leigh Syndrome and the m.10191T>C Mutation in MT-ND3

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A guide to diagnosis and treatment of Leigh syndrome

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The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndrome

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Late-adult onset Leigh syndrome

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Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency

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Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

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Adult Leigh Disease Without Failure to Thrive

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Clinical Manifestations in Children With Mitochondrial Diseases

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Mutations in ND Subunits of Complex I Are an Important Genetic Cause of Childhood Mitochondrial Encephalopathies

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Leigh Syndrome: Clinical and Neuroimaging Follow-Up

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Rolandic Mitochondrial Encephalomyelopathy and MT-ND3 Mutations

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Leigh and Leigh-Like Syndrome in Children and Adults

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