Gene: ND5

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Gene: ND6

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Gene: CYTB

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rs797045055 in ND5;ND6;CYTB gene and Dysarthria PMID 26633545 2016 Molecular diagnostic experience of whole-exome sequencing in adult patients.

rs797045055 in ND5;ND6;CYTB gene and Dystonia PMID 26633545 2016 Molecular diagnostic experience of whole-exome sequencing in adult patients.

rs199476107 in ND5;ND6;CYTB gene and Leigh Disease PMID 11781695 2001 An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.

rs199476107 in ND5;ND6;CYTB gene and MELAS Syndrome PMID 11781695 2001 An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.

rs199476106 in ND5;ND6;CYTB gene and Optic Atrophy, Hereditary, Leber PMID 9452107 1998 Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.

PMID 10447650 1999 Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.

PMID 1417830 1992 An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.

PMID 11133798 2001 The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.

PMID 8854108 1996 Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.