Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation (Q82674539)

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17 January 2020

title

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation (English)

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17 January 2020

author name string

Wanshi Cai

1

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17 January 2020

Qun Fu

2

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17 January 2020

Xiangtian Zhou

3

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17 January 2020

Jia Qu

4

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17 January 2020

Yi Tong

5

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17 January 2020

Min-Xin Guan

6

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17 January 2020

publication date

1 November 2008

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Journal of Genetics and Genomics

17 January 2020

published in

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17 January 2020

volume

35

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17 January 2020

issue

11

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17 January 2020

page(s)

649-655

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Sequence and organization of the human mitochondrial genome

17 January 2020

cites work

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Sequence and gene organization of mouse mitochondrial DNA

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MITOMAP: a human mitochondrial genome database--2004 update

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7 January 2021

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

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7 January 2021

The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: cryptic signals revealed by comparative analysis between vertebrates

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7 January 2021

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

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7 January 2021

The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family.

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7 January 2021

The epidemiology of Leber hereditary optic neuropathy in the North East of England

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7 January 2021

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy

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7 January 2021

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

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7 January 2021

mtDNA mutations increase tumorigenicity in prostate cancer

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7 January 2021

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy

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7 January 2021

Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation

1 reference

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7 January 2021

The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation

1 reference

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7 January 2021

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family

1 reference

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7 January 2021

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

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7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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7 January 2021

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss

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7 January 2021

10.1016/S1673-8527(08)60086-7

Identifiers

DOI

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17 January 2020

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