(Q46002900)

18 December 2017

title

Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia. (English)

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18 December 2017

Leber hereditary optic neuropathy

main subject

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Kang Wang

1

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18 December 2017

Yuji Takahashi

2

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18 December 2017

Zong-Liang Gao

3

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18 December 2017

Guo-Xiang Wang

4

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18 December 2017

Xian-Wen Chen

5

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18 December 2017

Jun Goto

6

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18 December 2017

Jin-Ning Lou

7

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18 December 2017

Shoji Tsuji

8

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18 December 2017

publication date

21 May 2009

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18 December 2017

published in

Neurogenetics

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18 December 2017

volume

10

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18 December 2017

issue

4

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18 December 2017

page(s)

337-345

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18 December 2017

New World relapsing fever Borrelia found in Ornithodoros porcinus ticks in central Tanzania

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-009-0194-0

A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-009-0194-0

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-009-0194-0

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia

21 January 2018

1 reference

12 December 2020

Sequence and organization of the human mitochondrial genome

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12 December 2020

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy

1 reference

12 December 2020

Molecular analyses of mtDNA deletion mutations in microdissected skeletal muscle fibers from aged rhesus monkeys.

1 reference

12 December 2020

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

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12 December 2020

Molecular evidence for hybridization of species in the genus Gallus except for Gallus varius

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12 December 2020

Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.

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12 December 2020

A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia

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12 December 2020

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

The complete mitochondrial genome of the wallaroo (Macropus robustus) and the phylogenetic relationship among Monotremata, Marsupialia, and Eutheria

1 reference

12 December 2020

Leber's disease and dystonia: a mitochondrial disease

1 reference

12 December 2020

Nonneutral evolution at the mitochondrial NADH dehydrogenase subunit 3 gene in mice

1 reference

12 December 2020

Complete mitochondrial DNA sequences of six snakes: phylogenetic relationships and molecular evolution of genomic features

1 reference

12 December 2020

The mitochondrial DNA of the amoeboid protozoon, Acanthamoeba castellanii: complete sequence, gene content and genome organization

1 reference

12 December 2020

Leber's hereditary optic neuropathy with dystonia in a Japanese family

1 reference

12 December 2020

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

1 reference

12 December 2020

Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation.

1 reference

12 December 2020

Unexpected species diversity of Malagasy primates (Lepilemur spp.) in the same biogeographical zone: a morphological and molecular approach with the description of two new species

1 reference

12 December 2020

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

1 reference

12 December 2020

A MELAS-Associated ND1 Mutation Causing Leber Hereditary Optic Neuropathy and Spastic Dystonia

1 reference

12 December 2020

Out of Hawaii: the origin and biogeography of the genus Scaptomyza (Diptera: Drosophilidae)

1 reference

12 December 2020

Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations

1 reference

12 December 2020

A novel mitochondrial genome organization for the blue mussel, Mytilus edulis

1 reference

12 December 2020

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

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12 December 2020

Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy

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12 December 2020

Sequence analysis of Hungarian LHON patients not carrying the common primary mutations

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12 December 2020

Familial dystonia and visual failure with striatal CT lucencies

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12 December 2020

High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy

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12 December 2020

Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families

1 reference

12 December 2020

Evolutionary history of the European whitefish Coregonus lavaretus (L.) species complex as inferred from mtDNA phylogeography and gill-raker numbers

1 reference

12 December 2020

10.1007/S10048-009-0194-0

Identifiers

DOI

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18 December 2017

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18 December 2017