Pages that link to "Q48183315"
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The following pages link to Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene (Q48183315):
Displayed 31 items.
- A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine (Q29547303) (← links)
- Brain mechanisms of acoustic communication in humans and nonhuman primates: an evolutionary perspective (Q30010598) (← links)
- Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature. (Q30910075) (← links)
- Neurological Disorders Associated with Striatal Lesions: Classification and Diagnostic Approach. (Q31076462) (← links)
- Pediatric-onset dystonia associated with bilateral striatal necrosis and G14459A mutation in a Korean family: a case report (Q33565423) (← links)
- Parkinson's disease in relation to pesticide exposure and nuclear encoded mitochondrial complex I gene variants (Q34795226) (← links)
- mtDNA Mutations and Their Role in Aging, Diseases and Forensic Sciences (Q35059486) (← links)
- Mitochondrial mutations are associated with atherosclerotic lesions in the human aorta (Q36246980) (← links)
- Convergent mechanisms in etiologically-diverse dystonias (Q36445234) (← links)
- Association of mitochondrial genetic variation with carotid atherosclerosis (Q36997420) (← links)
- The neurologic manifestations of mitochondrial disease (Q37785511) (← links)
- POLG1-related and other "mitochondrial Parkinsonisms": an overview. (Q37827400) (← links)
- Mutations in ND subunits of complex I are an important genetic cause of childhood mitochondrial encephalopathies (Q38493565) (← links)
- microRNA-mediated differential expression of TRMU, GTPBP3 and MTO1 in cell models of mitochondrial-DNA diseases (Q38663607) (← links)
- Nuclear suppression of mitochondrial defects in cells without the ND6 subunit (Q40326435) (← links)
- Modification of spectral features by nonhuman primates (Q41152831) (← links)
- Leigh disease presenting in utero due to a novel missense mutation in the mitochondrial DNA-ND3. (Q43142772) (← links)
- Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family (Q45765596) (← links)
- PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy. (Q47879508) (← links)
- Adult-onset chorea and mitochondrial cytopathy (Q47880350) (← links)
- Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case (Q48610555) (← links)
- Near-identical segregation of mtDNA heteroplasmy in blood, muscle, urinary epithelium, and hair follicles in twins with optic atrophy, ptosis, and intractable epilepsy. (Q48933024) (← links)
- Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene. (Q51187485) (← links)
- A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1. (Q52840797) (← links)
- Association of mitochondrial mutations with the age of patients having atherosclerotic lesions. (Q53276957) (← links)
- A De Novo Mutation in MTND6 Causes Generalized Dystonia in 2 Unrelated Children. (Q53293802) (← links)
- Mitochondrial DNA mutation 14487T>C manifesting as Leber’s hereditary optic neuropathy (Q56899885) (← links)
- Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation (Q64263368) (← links)
- Bilateral striatal necrosis due to homoplasmic mitochondrial 3697G>A mutation presents with incomplete penetrance and sex bias (Q64264933) (← links)
- Systematic analysis of a mitochondrial disease-causing ND6 mutation in mitochondrial deficiency (Q90257792) (← links)
- Mitochondrial dysfunction and its role in tissue-specific cellular stress (Q92932334) (← links)