Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy

scientific article published on February 1, 1992

Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy is …
instance of (P31):
scholarly articleQ13442814

External links are
P953full work available at URLhttps://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
P932PMC publication ID1682448
P698PubMed publication ID1734726

P2093author name stringD. McCullough
I. Bodis-Wollner
N. Howell
P2860cites workLeber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigreesQ24678456
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathyQ24678885
Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutationQ24679168
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathyQ28292821
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 neuroretinopathyQ35198232
An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 geneQ35198332
LEBER'S DISEASE IN THE NETHERLANDS.Q35453847
Rapid segregation of heteroplasmic bovine mitochondriaQ35946164
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 mutationQ48706853
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 pedigreesQ69197416
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathyQ69369711
The clinical findings in Leber's hereditary optic neuroretinopathy. Leber's diseaseQ69878988
P433issue2
P407language of work or nameEnglishQ1860
P304page(s)443-446
P577publication date1992-02-01
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titleMolecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy
P478volume50

Reverse relations

cites work (P2860)
Q42559012A heteroplasmic LHON family: tissue distribution and transmission of the 11778 mutation.
Q34162305Familial identification: population structure and relationship distinguishability
Q35882223Heteroplasmic point mutations in the human mtDNA control region.
Q35881405Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing
Q36581411Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck
Q40697792Mitochondrial encephalomyopathies: clinical and molecular analysis
Q43586519Mitochondrial gene segregation in mammals: is the bottleneck always narrow?
Q44338449Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy
Q42558990Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy.
Q43146868When does bilateral optic atrophy become Leber hereditary optic neuropathy?

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