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Authors: V. Carelli
Journal Article
Multi-system neurological disease is common in patients with OPA1 mutations Open Access
Brain, Volume 133, Issue 3, March 2010, Pages 771–786, https://doi.org/10.1093/brain/awq007
Published: 15 February 2010
Journal Article
`Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation Get access
Brain, Volume 123, Issue 9, September 2000, Pages 1896–1902, https://doi.org/10.1093/brain/123.9.1896
Published: 01 September 2000
