(Q48956364)

17 February 2018

title

Mitochondrial DNA and RNA processing in MELAS. (English)

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17 February 2018

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Kaufmann P

1

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17 February 2018

Koga Y

2

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17 February 2018

Shanske S

3

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17 February 2018

Hirano M

4

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17 February 2018

DiMauro S

5

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17 February 2018

King MP

6

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17 February 2018

Schon EA

7

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17 February 2018

publication date

1 August 1996

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17 February 2018

published in

Annals of Neurology

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17 February 2018

volume

40

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17 February 2018

issue

2

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17 February 2018

page(s)

172-180

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17 February 2018

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

cites work

1 reference

https://api.crossref.org/works/10.1002%2FANA.410400208

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410400208

Characterization and Localization of the Human Genes for Ribosomal Ribonucleic Acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410400208

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410400208

In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410400208

21 January 2018

Identifiers

DOI

10.1002/ANA.410400208

1 reference

17 February 2018

1 reference

17 February 2018