Pages that link to "Q43216889"

The following pages link to mtDNA mutations that cause optic neuropathy: how do we know? (Q43216889):

Displaying 25 items.

• The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates (Q24531956) (← links)
• The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs (Q24540081) (← links)
• The epidemiology of Leber hereditary optic neuropathy in the North East of England (Q24611047) (← links)
• The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme (Q28368398) (← links)
• Persistent heteroplasmy of a mutation in the human mtDNA control region: hypermutation as an apparent consequence of simple-repeat expansion/contraction (Q28768415) (← links)
• Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy (Q31081831) (← links)
• Mitochondrial encephalomyopathies: the enigma of genotype versus phenotype (Q33540911) (← links)
• Clinical, biochemical and molecular genetic features of Leber's hereditary optic neuropathy (Q33540913) (← links)
• Leber hereditary optic neuropathy (Q34118893) (← links)
• Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside (Q34495453) (← links)
• The role of the Met98Lys optineurin variant in inherited optic nerve diseases (Q35762674) (← links)
• Development and validation of a novel PCR-RFLP based method for the detection of 3 primary mitochondrial mutations in Leber's hereditary optic neuropathy patients (Q36310976) (← links)
• Inherited mitochondrial optic neuropathies (Q37098009) (← links)
• A real-time ARMS PCR/high-resolution melt curve assay for the detection of the three primary mitochondrial mutations in Leber's hereditary optic neuropathy (Q37337164) (← links)
• Novel therapeutic approaches for Leber's hereditary optic neuropathy (Q38094802) (← links)
• Nuclear suppression of mitochondrial defects in cells without the ND6 subunit (Q40326435) (← links)
• An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome (Q43848169) (← links)
• Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy. (Q44060092) (← links)
• A high frequency of mtDNA polymorphisms in HeLa cell sublines (Q46864338) (← links)
• Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene. (Q51187485) (← links)
• Different Patterns of Expansion/Contraction During the Evolution of an mtDNA Simple Repeat (Q57252182) (← links)
• Chapter 4 Leber's Hereditary Optic Neuropathy (Q57721287) (← links)
• Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve (Q74783603) (← links)
• Human mitochondrial diseases: answering questions and questioning answers (Q77403432) (← links)
• Mitochondrial encephalomyopathies (Q82029875) (← links)