| P50 | author | Monica Sciacco | Q80074726 |
| P2093 | author name string | E. A. Schon | |
| | X. Chen | |
| | E. Bonilla | |
| P2860 | cites work | A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 |
| | Sequence and organization of the human mitochondrial genome | Q27860659 |
| | Deletions of mitochondrial DNA in Kearns-Sayre syndrome | Q28297900 |
| | Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysis | Q34196561 |
| | Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain. | Q34343198 |
| | Detection of a specific mitochondrial DNA deletion in tissues of older humans | Q35891834 |
| | Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA. | Q35907687 |
| | A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues | Q37147048 |
| | Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome | Q41777128 |
| | A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA. | Q41951578 |
| | Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence | Q44498466 |
| | Preferential loss of striato-external pallidal projection neurons in presymptomatic Huntington's disease | Q45291252 |
| | Evidence for a defect in NADH: ubiquinone oxidoreductase (complex I) in Huntington's disease | Q45294442 |
| | Increased proteins in post-mortem brain in a case of Pick's disease and in Huntington's disease | Q45297302 |
| | Quantitative study of gliosis in schizophrenia and Huntington's chorea | Q45299045 |
| | Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain | Q45948111 |
| | Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome | Q46963412 |
| | Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age | Q48403808 |
| | Quantitation of a mitochondrial DNA deletion in Parkinson's disease | Q48507765 |
| | Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies | Q59055292 |
| | Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome | Q63681446 |
| | Abnormalities of the electron transport chain in idiopathic Parkinson's disease | Q69361952 |
| | Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases | Q69368213 |
| | Mitochondrial involvement in Parkinson's disease: the controversy continues | Q72586491 |
| | Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patients | Q72586534 |
| | Cytochrome C oxidase deficiency and neuronal involvement in Menkes' kinky hair disease: immunohistochemical study | Q72736191 |
| | Cloning of human mitochondrial DNA in Escherichia coli | Q72863042 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Huntington's disease | Q190564 |
| | sequence deletion | Q70689645 |
| P304 | page(s) | 229-233 | |
| P577 | publication date | 1995-05-01 | |
| | 1995-05-24 | |
| P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
| P1476 | title | Paucity of deleted mitochondrial DNAs in brain regions of Huntington's disease patients | |
| P478 | volume | 1271 | |