scholarly article | Q13442814 |
P953 | full work available at URL | https://europepmc.org/articles/PMC1682448 |
https://europepmc.org/articles/PMC1682448?pdf=render | ||
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1734726/?tool=EBI | ||
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1734726/pdf/?tool=EBI | ||
P932 | PMC publication ID | 1682448 |
P698 | PubMed publication ID | 1734726 |
P2093 | author name string | D. McCullough | |
I. Bodis-Wollner | |||
N. Howell | |||
P2860 | cites work | Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees | Q24678456 |
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy | Q24678885 | ||
Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation | Q24679168 | ||
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy | Q28292821 | ||
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy. | Q33593412 | ||
Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy | Q35198232 | ||
An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene | Q35198332 | ||
LEBER'S DISEASE IN THE NETHERLANDS. | Q35453847 | ||
Rapid segregation of heteroplasmic bovine mitochondria | Q35946164 | ||
Variable genotype of Leber's hereditary optic neuropathy patients. | Q41730723 | ||
Does sporadic Leber's disease exist? | Q43897489 | ||
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation | Q48706853 | ||
Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy. | Q52240438 | ||
Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees | Q69197416 | ||
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy | Q69369711 | ||
The clinical findings in Leber's hereditary optic neuroretinopathy. Leber's disease | Q69878988 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 443-446 | |
P577 | publication date | 1992-02-01 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy | |
P478 | volume | 50 |
Q42559012 | A heteroplasmic LHON family: tissue distribution and transmission of the 11778 mutation. |
Q34162305 | Familial identification: population structure and relationship distinguishability |
Q35882223 | Heteroplasmic point mutations in the human mtDNA control region. |
Q35881405 | Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing |
Q36581411 | Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck |
Q40697792 | Mitochondrial encephalomyopathies: clinical and molecular analysis |
Q43586519 | Mitochondrial gene segregation in mammals: is the bottleneck always narrow? |
Q44338449 | Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy |
Q42558990 | Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy. |
Q43146868 | When does bilateral optic atrophy become Leber hereditary optic neuropathy? |
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