(Q48836050)

16 February 2018

title

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. (English)

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16 February 2018

author name string

Goto Y

series ordinal

1

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16 February 2018

Nonaka I

series ordinal

2

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16 February 2018

Horai S

series ordinal

3

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16 February 2018

language of work or name

English

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publication date

1 December 1990

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16 February 2018

published in

Nature

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16 February 2018

volume

348

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16 February 2018

issue

6302

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16 February 2018

page(s)

651-653

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16 February 2018

cites work

Mitochondrial myopathies

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7 January 2021

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

7 January 2021

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

1 reference

7 January 2021

Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block

1 reference

7 January 2021

A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. I. Clinical, pathologic and biochemical characteristics

1 reference

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

7 January 2021

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

7 January 2021

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

7 January 2021

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome

1 reference

7 January 2021

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.

1 reference

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

7 January 2021

Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome

1 reference

7 January 2021

Sequence and gene organization of mouse mitochondrial DNA

1 reference

7 January 2021

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

1 reference

7 January 2021

Sequence and gene organization of the chicken mitochondrial genome. A novel gene order in higher vertebrates

1 reference

7 January 2021

The mitochondrial DNA molecular of Drosophila yakuba: nucleotide sequence, gene organization, and genetic code

1 reference

7 January 2021

Nucleotide sequence and gene organization of sea urchin mitochondrial DNA.

1 reference

7 January 2021

Transfer RNA: Molecular Structure, Sequence, and Properties

1 reference

7 January 2021

Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus

1 reference

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

7 January 2021

Identifiers

DOI

10.1038/348651A0

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16 February 2018

Dimensions Publication ID

1027941299

0 references

1 reference

16 February 2018