Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.

Literature DB >> 8417984

Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.

N Howell, I Kubacka, S Halvorson, D Mackey.

Abstract

Entities: Disease Gene

Mesh：

Substances：
Cytochrome b Group

Year: 1993 PMID： 8417984 PMCID： PMC1205293

Source DB: PubMed Journal: Genetics ISSN： 0016-6731 Impact factor: 4.562

Keyword Cloud
Cited

× No keyword cloud information.

15 in total

1. Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

Authors: D A Mackey; R J Oostra; T Rosenberg; E Nikoskelainen; J Bronte-Stewart; J Poulton; A E Harding; G Govan; P A Bolhuis; S Norby
Journal: Am J Hum Genet Date: 1996-08 Impact factor: 11.025

2. Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations.

Authors: S Hofmann; R Bezold; M Jaksch; P Kaufhold; B Obermaier-Kusser; K D Gerbitz
Journal: Am J Hum Genet Date: 1997-06 Impact factor: 11.025

3. When does bilateral optic atrophy become Leber hereditary optic neuropathy?

Authors: N Howell; S Halvorson; J Burns; D A McCullough; J Paulton
Journal: Am J Hum Genet Date: 1993-10 Impact factor: 11.025

Review 4. Molecular basis of mitochondrial DNA disease.

Authors: M D Brown; D C Wallace
Journal: J Bioenerg Biomembr Date: 1994-06 Impact factor: 2.945

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

Authors: R J Oostra; P A Bolhuis; I Zorn-Ende; M M de Kok-Nazaruk; E M Bleeker-Wagemakers
Journal: Hum Genet Date: 1994-09 Impact factor: 4.132

Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.

1. Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

2. Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations.

3. When does bilateral optic atrophy become Leber hereditary optic neuropathy?

Review 4. Molecular basis of mitochondrial DNA disease.

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

6. Mitochondrial gene mutations and human diseases: a prolegomenon.

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

Review 8. Leber hereditary optic neuropathy: how do mitochondrial DNA mutations cause degeneration of the optic nerve?

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

Review 10. Mitochondrial DNA sequence variation in human evolution and disease.