Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation (Q28217558)

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scientific article (publication date: 26 July 2002)

Language	Label	Description	Also known as
English	Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation	scientific article (publication date: 26 July 2002)

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scholarly article

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Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation (English)

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based on heuristic

inferred from title

Mitochondrial tRNA translation optimization 1

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GOA release 2020-03-11

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based on heuristic

inferred from title

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based on heuristic

inferred from title

author name string

Xiaoming Li

1

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Ronghua Li

2

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Xinhua Lin

3

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Min-Xin Guan

4

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language of work or name

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publication date

26 July 2002

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Journal of Biological Chemistry

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277

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30

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27256-64

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Mitochondrial DNA mutations and pathogenesis

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Mitochondrial diseases in man and mouse

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Mitochondrial deafness mutations reviewed

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Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.

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Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

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Identifiers

10.1074/JBC.M203267200

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