Leucine

mitochondrially encoded NADH dehydrogenase 1 ; Homo sapiens







3 Article(s)
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1 22553750 Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutation. 2012 1
2 12112111 Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis. 2002 May 1
3 2018041 Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation. 1991 May 1