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Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

published in: American Journal of Human Genetics

date of publication: 1997-02-01

language: English

main subject: patient, Leber hereditary optic neuropathy

Cites articles 16

Date

Title

Authors

1995-01-01

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations
1995-05-01

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees
1995-07-01

Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation

Mary G. Sweeney
1995-04-01

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

Mary G. Sweeney
1995-01-01

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

David Curtis
1994-04-01

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome

Roelof-Jan Oostra
1994-11-01

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy

Thomas Meitinger
1994-10-01

mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region
1994-09-01

Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation

Roelof-Jan Oostra
1993-05-01

Leber's hereditary optic neuropathy. New genetic considerations
1993-04-01

Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation
1993-10-01

The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy
1992-01-01

Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy
1992-08-01

Leber hereditary optic neuropathy in Australia
1992-09-30

An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy
1991-02-14

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

Article - wd:Q42037714

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