Pages that link to "Q73056557"

The following pages link to Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes (Q73056557):

Displaying 31 items.

• A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome) (Q22003951) (← links)
• Human mtDNA haplogroups associated with high or reduced spermatozoa motility (Q24538797) (← links)
• Leber's hereditary optic neuropathy is multiorgan not mono-organ (Q28067201) (← links)
• Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice (Q28863937) (← links)
• A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy (Q33681493) (← links)
• Male sperm motility dictated by mother's mtDNA (Q34142571) (← links)
• Mitochondria, aging and longevity--a new perspective. (Q34180529) (← links)
• The neuro-ophthalmology of mitochondrial disease (Q34338783) (← links)
• Mitochondria in the pathogenesis of lipodystrophy induced by anti-HIV antiretroviral drugs: actors or bystanders? (Q34464649) (← links)
• Mitochondrial DNA haplogroups confer differences in risk for age-related macular degeneration: a case control study. (Q34542987) (← links)
• Two families with autosomal dominant progressive external ophthalmoplegia (Q35482241) (← links)
• Female genetic distribution bias in mitochondrial genome observed in Parkinson's Disease patients in northern China. (Q36316602) (← links)
• Specific polymorphic variation in the mitochondrial genome and increased in-hospital mortality after severe trauma (Q36918606) (← links)
• Pharmacogenetics of nucleoside reverse-transcriptase inhibitor-associated peripheral neuropathy (Q37251569) (← links)
• Wolfram syndrome and WFS1 gene (Q37782389) (← links)
• Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient. (Q38932064) (← links)
• Resistance of mtDNA-depleted cells to apoptosis (Q40008780) (← links)
• Recent developments in the molecular genetics of mitochondrial disorders (Q41725491) (← links)
• Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations (Q43104709) (← links)
• The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy (Q45472883) (← links)
• No mitochondrial haplotype was found to increase risk for Alzheimer's disease. (Q50864482) (← links)
• Mito-Nuclear Interactions Affecting Lifespan and Neurodegeneration in a Drosophila Model of Leigh Syndrome (Q51736760) (← links)
• WFS1/wolframin mutations, Wolfram syndrome, and associated diseases (Q56803820) (← links)
• Genetic Aspects of Keratoconus: A Literature Review Exploring Potential Genetic Contributions and Possible Genetic Relationships with Comorbidities. (Q64987781) (← links)
• Population Genetics and Disease Susceptibility: Characterization of Central European Haplogroups By mtDNA Gene Mutations, Correlation with D Loop Variants and Association With Disease (Q73709402) (← links)
• Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians (Q74554779) (← links)
• [Wolfram's syndrome presenting as a cerebellar ataxia] (Q79918859) (← links)
• The mitochondrial pharmacogenomics of haplogroup T: MTND2*LHON4917G and antiretroviral therapy-associated peripheral neuropathy (Q80761703) (← links)
• Hereditary optic neuropathies (Q80981275) (← links)
• The novel compound heterozygous mutations, V434del and W666X, in WFS1 gene causing the Wolfram syndrome in a Chinese family (Q83217870) (← links)
• Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!! (Q83956779) (← links)